Emmes Group

JOB_DESCRIPTION.SHARE.HTML CAROUSEL_PARAGRAPH JOB_DESCRIPTION.SHARE.HTML India - Bengaluru Information Technology No Regular Full-Time 2545 Emmes Global mail_outline Get future jobs matching this search or Overview Job Description Emmes Group: Building a better future for us all. OptymEdge is a global leader in ophthalmic endpoint certification, partnering with leading biopharma sponsors and CROs to ensure the quality and consistency of visual function data in clinical trials. With a reputation built on scientific expertise, operational excellence, and global delivery, we’ve become a trusted name in advancing treatments for sight-threatening diseases. As the field evolves, so do we. OptymEdge is expanding into technology-driven product development , creating a new generation of platforms that redefine how ophthalmic data is captured, analyzed, and leveraged across the clinical trial lifecycle. Our innovations span AI-powered imaging, digital examiner certification, and intelligent operational tools designed to anticipate trial needs, streamline oversight, and enhance decision-making. This is a rare opportunity to help shape transformative technology at the intersection of science, software, and sight—driving real-world impact in a field where every data point can influence patient vision. Primary Purpose We are hiring a Product Owner with 5–8 years of experience to lead the roadmap, definition, and delivery of digital products powering ophthalmic imaging and certification platforms in global clinical trials. This role bridges scientific insight, user needs, and technical delivery to shape product experiences that are clinically meaningful and operationally scalable. You will work closely with engineering, clinical operations, product management, business partners, and sponsors to deliver products that meet rigorous quality standards in a fast-paced, mission-driven environment. Responsibilities Own the product backlog for one or more AI-driven imaging or certification platforms. Translate user and clinical requirements into detailed epics, user stories, and acceptance criteria. Collaborate closely with engineering, data engineering, QA, and operations teams to deliver timely and validated releases. Drive agile ceremonies including backlog grooming, sprint planning, and release retrospectives. Ensure alignment with regulatory-grade workflows (21 CFR Part 11, HIPAA) in trial-facing tools. Coordinate with business users, product managers and internal SMEs to validate roadmap priorities. Define and track key product KPIs including user engagement, system accuracy, and time-to-grade. Work across internal teams to ensure UAT readiness, documentation, and training plans are in place. Support the long-term roadmap for imaging platforms, grader workflows, and intelligent operational tools. Qualifications Bachelor’s or Master’s degree in Engineering, Life Sciences, or a related field. 5–8 years of experience in product management or product ownership in digital health, imaging, clinical tech or any healthcare sector. Strong working knowledge of agile frameworks and product lifecycle best practices. Ability to work with UX/UI designers, backend/frontend engineers, SQA and Product Managers. Hands-on experience writing clear and testable user stories and managing cross-functional sprint execution. Familiarity with healthcare data standards (e.g., DICOM, FHIR) and medical imaging workflows is desired Experience working in regulated environments (GCP, HIPAA, 21 CFR Part 11) is a strong plus. Exposure to clinical trials, especially ophthalmology or radiology, is highly preferred. Customer-obsessed with a bias for clarity and usability. Strong analytical and systems-thinking skills. Excellent communicator – crisp in writing, clear in meetings. Comfortable balancing strategic vision with tactical detail. High ownership mindset with startup agility. CONNECT WITH US! Follow us on Twitter - @EmmesCRO Find us on LinkedIn - Emmes Show more Show less

JOB_DESCRIPTION.SHARE.HTML CAROUSEL_PARAGRAPH JOB_DESCRIPTION.SHARE.HTML India - Bengaluru Clinical Operations Yes Regular Full-Time 2414 Emmes Global mail_outline Get future jobs matching this search or Overview Job Description CRA II India Remote/Ahmedabad/Bengaluru/New Delhi Emmes Group: Building a better future for us all. Emmes Group is transforming the future of clinical research, bringing the promise of new medical discovery closer within reach for patients. Emmes Group was founded as Emmes more than 47 years ago, becoming one of the primary clinical research providers to the US government before expanding into public-private partnerships and commercial biopharma. Emmes has built industry leading capabilities in cell and gene therapy, vaccines and infectious diseases, ophthalmology, rare diseases, and neuroscience. We believe the work we do will have a direct impact on patients’ lives and act accordingly. We strive to build a collaborative culture at the intersection of being a performance and people driven company. We’re looking for talented professionals eager to help advance clinical research as we work to embed innovation into the fabric of our company. If you share our motivations and passion in research, come join us! Primary Purpose The Clinical Research Associate (CRA) II is responsible for monitoring clinical study sites either onsite at investigative sites or remotely to ensure clinical trials are conducted, recorded, and reported in accordance with the protocol, standard operating procedures (SOPs), ICH GCP, and all applicable regulatory requirements. The CRA will conduct monitoring visits and activities in accordance with Emmes SOPs, applicable regulations, and ICH GCP. Responsibilities Under supervision of the project CRA staff oversight lead (i.e. Clinical Study Manager, Lead CRA, Project Manager, etc.), independently schedules and conducts remote and on-site monitoring visits such as qualification/pre-study visits, site initiation visits, interim/routine monitoring visits, closeout visits, and for-cause visits. As part of the site visits, independently conducts Informed Consent (ICF) review, source data verification/source document review, review for compliance with required reporting/tracking of adverse events and protocol deviations, investigator site file review, laboratory tour and specimen storage assessment, pharmacy/Investigational Product (IP)/Investigational Device (ID) storage location tour and storage condition assessment, IP/ID accountability, facilities tours, and other activities per the site monitoring plan under minimal direction from the project CRA staff oversight lead. Documents observations and monitoring activities in a site visit report at the conclusion of the visit. Facilitates and oversees Action Item resolution post visit. Helps to ensure that clinical sites are conducting the study in compliance with protocol/clinical investigational plan, SOPs, ICH GCP, and other applicable regulations. Provides training and retraining to site staff including protocol, GCP/GDP, and other training under direction from the project CRA staff oversight lead. Identifies areas requiring follow-up and improvement at each clinical study site and reports findings to project CRA staff oversight lead. Ensures all visits are conducted according to country regulations, ICH GCP, and company standard operating procedures Serves as point of contact for study site personnel to answer questions and resolve study related issues under the direction of the project CRA staff oversight lead. May assist with the development and/or review of study-related materials including protocols, informed consent forms, monitoring plan, monitoring documents, etc. Prepares for and attends project team meetings and provides updates on project status and site-specific performance Works collaboratively and effectively in a project team environment including internal and external colleagues to meet project objectives and timelines Participates in Investigator Meetings or other client meetings as needed Assists with filing and archiving of study documents Assists in preparing sites for audits and may provide support and cooperation during audits/inspections (including translation to Auditor if needed) May assist with coordination of clinical study supplies May assist with submission of applications/notifications to Institutional Review Board (IRB)/Ethics Committee (EC)/Regulatory Authority May assist with site recruitment oversight activities such as developing focused patient recruitment strategies and action plans. Performs site management activities as required Other duties as assigned Qualifications Bachelor’s degree (scientific discipline preferred) or equivalent work experience At least 1-2 years of relevant monitoring experience (on-site and remote) Proficient with MS Office Suite Excellent computer and organizational skills High level of attention to detail required Ability to work on varying projects and exercise critical thinking Self-starter who can work remotely and a team player who can work cross functionally with some oversight Knowledgeable in clinical research operations, including interpretation and implementation of country regulations/ICH guidelines, as required per their role as a CRA Excellent organizational, interpersonal, and communication skills (both oral and written) Demonstrated problem-solving skills, self-motivated, and adaptable to a dynamic environment Knowledgeable in prioritization, problem-solving, organization, critical thinking, decisionmaking, time management, and planning activities \ Ability to collaborate with internal and external colleagues and work well in a team-oriented setting CONNECT WITH US! 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Design, build, and optimize interactive image viewers for Ophthalmologic Imaging solution Develop robust annotation tools supporting manual segmentation, labeling, corrections, and metadata capture. Implement image upload/download workflows, versioning, session handling, and data security. Collaborate with AI Imaging Engineers to integrate segmentation outputs into the viewer and annotation modules. Work with Backend Engineers to define and consume secure APIs for imaging data management. Ensure clinical-grade performance for large image sets (responsive, low-latency frontend experience). Write clean, maintainable, and well-documented code following software engineering best practices. Overview Emmes Group: Building a better future for us all. Emmes Group is transforming the future of clinical research, bringing the promise of new medical discovery closer within reach for patients. Emmes Group was founded as Emmes more than 47 years ago, becoming one of the primary clinical research providers to the US government before expanding into public-private partnerships and commercial biopharma. Emmes has built industry leading capabilities in cell and gene therapy, vaccines and infectious diseases, ophthalmology, rare diseases, and neuroscience. We believe the work we do will have a direct impact on patients lives and act accordingly. We strive to build a collaborative culture at the intersection of being a performance and people driven company. We re looking for talented professionals eager to help advance clinical research as we work to embed innovation into the fabric of our company. If you share our motivations and passion in research, come join us! OptymEdge is a global leader in ophthalmic endpoint certification, partnering with leading biopharma sponsors and CROs to ensure the quality and consistency of visual function data in clinical trials. With a reputation built on scientific expertise, operational excellence, and global delivery, we ve become a trusted name in advancing treatments for sight-threatening diseases. As the field evolves, so do we. OptymEdge is expanding into technology-driven product development, creating a new generation of platforms that redefine how ophthalmic data is captured, analyzed, and leveraged across the clinical trial lifecycle. Our innovations span AI-powered imaging, digital examiner certification, and intelligent operational tools designed to anticipate trial needs, streamline oversight, and enhance decision-making. This is a rare opportunity to help shape transformative technology at the intersection of science, software, and sight driving real-world impact in a field where every data point can influence patient vision. Primary Purpose We are seeking a Senior Software Engineer with 5-7 years of experience to design, develop, and optimize advanced Ophthalmology imaging applications. You will play a critical role in developing the Image viewer, annotation tools, image management workflows, and frontend-backend integration necessary for a scalable, clinical-grade ophthalmology imaging system. You will work closely with product, clinical, and engineering teams in an agile environment to deliver innovative, production-grade imaging solutions that redefine clinical outcomes. Responsibilities Design, build, and optimize interactive image viewers for Ophthalmologic Imaging solution Develop robust annotation tools supporting manual segmentation, labeling, corrections, and metadata capture. Implement image upload/download workflows, versioning, session handling, and data security. Collaborate with AI Imaging Engineers to integrate segmentation outputs into the viewer and annotation modules. Work with Backend Engineers to define and consume secure APIs for imaging data management. Ensure clinical-grade performance for large image sets (responsive, low-latency frontend experience). Write clean, maintainable, and well-documented code following software engineering best practices. Qualifications Bachelor s or Master s degree in Computer Science, Software Engineering, or a related field. 5-7 years of professional software development experience building full-stack or frontend applications. Strong expertise in ReactJS (hooks, state management, component design) and modern frontend frameworks. Experience working with WebGL, Canvas, or advanced rendering libraries for imaging applications. Solid backend integration experience with RESTful APIs or GraphQL. Working knowledge of Python services (Flask/FastAPI) for API communication (you dont need to be a Python backend expert, but you should know how to consume and work with it). Exposure to handling large imaging files (DICOM, TIFF etc.) and browser-based optimization techniques. Understanding of basic cloud concepts (AWS S3, Cloudfront, Authentication flows) CONNECT WITH US! Follow us on Twitter - @EmmesCRO Find us on LinkedIn - Emmes

JOB_DESCRIPTION.SHARE.HTML CAROUSEL_PARAGRAPH JOB_DESCRIPTION.SHARE.HTML India - Bengaluru Medical & Safety No Regular Full-Time 2524 Emmes Global mail_outline Get future jobs matching this search or Overview Job Description Emmes Group: Building a better future for us all. Emmes Group is transforming the future of clinical research, bringing the promise of new medical discovery closer within reach for patients. Emmes Group was founded as Emmes more than 47 years ago, becoming one of the primary clinical research providers to the US government before expanding into public-private partnerships and commercial biopharma. Emmes has built industry leading capabilities in cell and gene therapy, vaccines and infectious diseases, ophthalmology, rare diseases, and neuroscience. We believe the work we do will have a direct impact on patients’ lives and act accordingly. We strive to build a collaborative culture at the intersection of being a performance and people driven company. We’re looking for talented professionals eager to help advance clinical research as we work to embed innovation into the fabric of our company. If you share our motivations and passion in research, come join us! Primary Purpose The Safety Monitor II will implement Pharmacovigilance activities in collaboration with other members of the Pharmacovigilance and Medical Monitoring (PMM) department, under general supervision. The Safety Monitor II will assist senior level Safety Monitors with interventional and non-interventional clinical projects in conjunction with the assigned Medical Monitor/Medical Officer and the project team and may be assigned as the Primary Safety Monitor for small projects. In addition, the Safety Monitor II will assist with the designing and execution of the assigned Pharmacovigilance (PV) related projects (e.g., management of local or international PV systems for contracted Clients; PV supervision of RWE (Real World Evidence projects); etc.) in close cooperation with other Emmes roles, especially with Medical Officers/Medical Monitors (or other similar medical expert roles), Regulatory roles, etc. The Safety Monitor II will support the adherence to Good Clinical Practice (GCP), Good Pharmacovigilance Practice (GVP) and other relevant Pharmacovigilance requirements. Responsibilities Assists in performing safety monitoring activities in cooperation with project Medical Monitor/Medical Officer and other relevant project team members. Reviews safety events. Assists in the collection, assessment, monitoring, review and reporting of adverse drug reaction cases from all sources – clinical (both interventional and non-interventional), data sets analyzed in association with RWE projects, spontaneous reports, literature, etc. ▪ Provides first line evaluation of serious adverse events (SAEs). Communicates with site staff regarding reported AEs or SAEs to gather additional information. Prepares a summary narrative for each reported SAE suitable for Medical Monitor/Officer review, and inclusion in Data Safety Monitoring Board (DSMB) reports, regulatory submissions, and final study reports. Coordinates the timely completion and submission of required reports to health authorities and business partners. ▪ Maintains ongoing database of SAEs and reconciles SAEs in the database as needed. Reviews adverse events and/or other safety related data such as toxicities, concomitant medications and medical history, etc. for the study on a regular basis. Establishes direct communication with Client, investigator site staff, national and regional regulatory authorities, health professionals, pharmaceutical and other study partners, as necessary. Responds to site, Client, DSMB, or Medical Monitor/Officer requests for information regarding safety in clinical trials (both interventional and noninterventional). Participates in DSMB or other safety review committee (SRC) meetings, including Protocol Safety Review Team (PSRT) meetings, as necessary. Reviews and contributes to DSMB/SRC reports regarding safety; reviews and contributes to safety sections of annual as well as periodic safety reports. Coordinates with project staff. Participates in project team meetings for the planning, preparation, and development of all safety-related sections of protocols, study specific safety documents such as Safety Management Plan (SaMP), Manual of Operations (MOP), project Standard Operating Procedures (SOPs), and ancillary documents to ensure project compliance with corporate SOPs. Contributes to the development and implementation of safety-related Case Report Forms (CRF) and SaMP. Ensures maintenance of documentation required by both corporate and project SOPs. Participates in project process improvement and corporate quality assurance activities through Internal Quality Audit Team (IQAT) processes, project SOP and Compliance/Variance table development, participation in both internal and external audits, as well as professional development activities. Performs Medical Dictionary for Regulatory Activities (MedDRA) and World Health Organization (WHO) Drug coding, as applicable. Guarantees compliance and adherence to the quality standards. Contributes to the development and maintenance of departmental quality documents (e.g., SOPs) and other work practices as assigned. Maintains accurate reporting to relevant authorities, such as Food and Drug Administration (FDA), European Medicines Agency (EMA) etc. when applicable per client contract. Contributes to the verification that Quality Control processes are conducted in accordance with applicable written procedures. Completes all relevant professional training in the given scope and time frame. Participates in corporate activities such as corporate safety meetings/activities; annual SOP reviews; cross-department working groups dedicated to improvement of the work processes and development of innovative solutions and other relevant corporate initiatives. Performs other duties as assigned. Qualifications Bachelor’s degree in pharmacology, nursing or other scientific discipline is required with relevant experience in clinical practice (e.g., pharmacy, inpatient or outpatient healthcare facility, or clinical research center, etc.). At least 2 years of related experience in research or with a pharmaceutical company (CRO, SMO, pharma company, etc.) Experience in safety monitoring/pharmacovigilance is preferred. The readiness to work in a regulated environment and understanding of the Good “x” Practice (GxP) principles. Ability to learn and understand quickly. Consistency, quality, compliance and patient centricity respected as key values. Excellent clinical judgement and ability to communicate moderately complex clinical issues in a scientifically sound and understandable way. Detail-oriented with good organizational skills Ability to work as a team member and function on a cross-functional team. Excellent verbal and written communication skills. CONNECT WITH US! 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Designs, develops, and enhances cloud-based, SaaS web-based clinical trials applications. Collaborates with product, engineering, and software quality assurance (SQA) team members for integration, design, and verification in an agile environment. Adheres to best practices and Emmes quality standards for code security, optimization, and reusability. Uses established frameworks for a seamless user experience across platforms. Performs unit testing, debugging, and troubleshooting as needed to ensure quality of work. Performs code reviews, assesses regression impact for design changes, and completes technical documentation. Identifies opportunities for refactoring/reworking major modules and sees implementation through to deployment. Mentor and coach junior and mid-level developers, promoting a collaborative and learning-driven environment. Conduct regular code reviews, provide feedback, and foster a culture of continuous improvement. Overview Emmes Group: Building a better future for us all. Emmes Group is transforming the future of clinical research, bringing the promise of new medical discovery closer within reach for patients. Emmes Group was founded as Emmes more than 47 years ago, becoming one of the primary clinical research providers to the US government before expanding into public-private partnerships and commercial biopharma. Emmes has built industry leading capabilities in cell and gene therapy, vaccines and infectious diseases, ophthalmology, rare diseases, and neuroscience. We believe the work we do will have a direct impact on patients lives and act accordingly. We strive to build a collaborative culture at the intersection of being a performance and people driven company. We re looking for talented professionals eager to help advance clinical research as we work to embed innovation into the fabric of our company. If you share our motivations and passion in research, come join us! Primary Purpose Designs, develops, and enhances cloud-based, software-as-a-service (SaaS) web-based clinical trials applications. Responsibilities Designs, develops, and enhances cloud-based, SaaS web-based clinical trials applications. Collaborates with product, engineering, and software quality assurance (SQA) team members for integration, design, and verification in an agile environment. Adheres to best practices and Emmes quality standards for code security, optimization, and reusability. Uses established frameworks for a seamless user experience across platforms. Performs unit testing, debugging, and troubleshooting as needed to ensure quality of work. Performs code reviews, assesses regression impact for design changes, and completes technical documentation. Identifies opportunities for refactoring/reworking major modules and sees implementation through to deployment. Mentor and coach junior and mid-level developers, promoting a collaborative and learning-driven environment. Conduct regular code reviews, provide feedback, and foster a culture of continuous improvement. Qualifications B.E/MTech/MCA degree in a computer related field Required Skills/Abilities 6 or more years of related professional experience. Min 4 years of experience in ReactJS and JavaScript/Typescript Min 4 years of experience in web platform development tools like Node.js, Express, AWS Amplify, AWS Lambda, AppSync, and GraphQL Min 4 years of experience in working with any relational or No SQL database. Min 2 years of experience in leading a team of engineers Expertise in developing Single Page Applications (SPA) Expertise with authentication and data caching. Expertise in API security. Expertise with DynamoDB, Amazon Aurora, or other relational database management system Experience with source code repositories like AWS CodeCommit, Git/GitHub, or SVN Experience working in an agile team. Experience in managing and delegating tasks to fellow team members Strong collaboration skills with cross-functional teams to establish best design and user flows for applications. Strong multitasking, problem solving, and organizational skills. Proven ability to work independently and in a team environment. Any of the following additional technical skills would be a plus: Expertise with GraphQL clients like Apollo Experience with Material Design Experience with Material-UI or other front-end libraries Experience with responsive UI for different form-factors Experience with modern IDEs like VSCode, integrated plugins for version control, and code prettify (ESLint) Experience with testing frameworks such as React Testing Experience with ECS/Docker Experience with distributed/event-driven systems (like Kafka or Kinesis) CONNECT WITH US! Follow us on Twitter - @EmmesCRO Find us on LinkedIn - Emmes

Overview Job Posting Title India Remote/Ahmedabad/Bengaluru/New Delhi Emmes Group: Building a better future for us all Emmes Group is transforming the future of clinical research, bringing the promise of new medical discovery closer within reach for patients Emmes Group was founded as Emmes more than 47 years ago, becoming one of the primary clinical research providers to the US government before expanding into public-private partnerships and commercial biopharma Emmes has built industry leading capabilities in cell and gene therapy, vaccines and infectious diseases, ophthalmology, rare diseases, and neuroscience We believe the work we do will have a direct impact on patients lives and act accordingly We strive to build a collaborative culture at the intersection of being a performance and people driven company We re looking for talented professionals eager to help advance clinical research as we work to embed innovation into the fabric of our company If you share our motivations and passion in research, come join us! Primary Purpose Responsibilities Qualifications CONNECT WITH US! Follow us on Twitter - @EmmesCRO Find us on LinkedIn - Emmes #LI-Remote

Data for AI: Design and implement data pipelines specifically tailored for AI training and model development. Partner with AI data scientists and engineers to understand their data needs and ensure efficient data access. Implement data pre-processing and feature engineering techniques for optimal model performance. AWS expertise: Design,develop, and maintain data infrastructure on the AWS cloud platform, leveraging services like S3,Redshift, Glue, Lambda, and Kinesis. Build and maintain data lakes and warehouses optimized for AI workloads. Implement automated data transformations,cleansing, and validation processes to ensure data quality. Coding proficiency: Write code using Python,SQL, and other relevant programming languages, with a focus on libraries and frameworks commonly used in AI (e.g., TensorFlow, PyTorch). Automation and monitoring: Automate data pipelines using CI/CD tools and related techniques. Monitor and troubleshoot data pipelines for performance, reliability,and data quality issues. Overview The Emmes Company, LLC ( Emmes ) is a global, full-service Clinical Research Organization dedicated to excellence in supporting the advancement of public health and biopharmaceutical innovation. We believe in the power of truth, so much so that we named our company Emmes, which means truth. Through decades of experience we have learned that collaborative relationships thrive and human health benefits when truth is our compass. Our Character Achieves Results culture is driven by five key values that guide our actions in the way we conduct research and distinguish us as an organization: Integrity, Agility, Passion for Excellence, Collaborative Partnerships and Intellectual Curiosity. We are a trusted partner to clients who share our passion for improving public health in a world of ever-changing scientific research. If you share our motivations and passion in research, come join us! You will be joining a collaborative culture that empowers every Emmes employee from entry level through top executive to contribute to our clients success by sharing ideas openly and honestly. Primary Purpose Building and maintaining our data infrastructure on the AWS cloud platform, with a specific focus on supporting AI model training, development, and deployment. This includes designing, developing, and implementing data pipelines, ensuring the secure and efficient flow of data for our AI models. Responsibilities Data for AI: Design and implement data pipelines specifically tailored for AI training and model development. Partner with AI data scientists and engineers to understand their data needs and ensure efficient data access. Implement data pre-processing and feature engineering techniques for optimal model performance. AWS expertise: Design,develop, and maintain data infrastructure on the AWS cloud platform, leveraging services like S3,Redshift, Glue, Lambda, and Kinesis. Build and maintain data lakes and warehouses optimized for AI workloads. Implement automated data transformations,cleansing, and validation processes to ensure data quality. Coding proficiency: Write code using Python,SQL, and other relevant programming languages, with a focus on libraries and frameworks commonly used in AI (e.g., TensorFlow, PyTorch). Automation and monitoring: Automate data pipelines using CI/CD tools and related techniques. Monitor and troubleshoot data pipelines for performance, reliability,and data quality issues. Qualifications 5 to 8 years of experience as a Data Engineer or similar role,with a demonstrated experience in supporting data pipelines for AI applications and their data requirements. Proven experience with AWS services,including S3, Redshift, Glue, Lambda, and Kinesis. Strong experience with Python and SQL. Strong understanding of AI libraries and frameworks. Experience with data warehousing and data modeling concepts. Excellent problem-solving and analytical skills. Ability to work independently and as part of a collaborative team. Strong communication and collaboration skills. CONNECT WITH US! Follow us on Twitter - @EmmesCRO Find us on LinkedIn - The Emmes Company, LLC

Communicate with stakeholders to ensure mutual understanding of requirements and functional specifications Review business processes involving assigned business applications and develop optimization strategies, including gathering critical information from meetings with various stakeholders and producing useful reports Evaluate needs and determination of feasibility based on business application capabilities and process improvement standards Document and effectively communicate your efforts, insights, and recommendations, including conducting meetings and presentations to share ideas and findings Ensure assigned business applications and processes meet business needs and requirements through user acceptance testing Research and propose efficient and economical ways to improve processes and optimize efficiencies within the assigned business applications Develop relationships throughout the company and its affiliates Assist with creation of and update training documents related to assigned business applications Develop skills in multiple technical environments and grasp a variety of business processes Resolve support issues related to assigned business applications Supports adoption efforts and usage optimization related to assigned business applications Assist with development of communications (both in written and in presentation formats) that convey ideas and recommendations in a clear and convincing way related to assigned business applications Build vendor partnerships for assigned applications Provides coaching and training as needed for new or junior team members Assist with release management for assigned applications May serve as technical owner of assigned applications May participate in validation activities as needed Other duties as assigned Overview Job Posting Title India Remote/Ahmedabad/Bengaluru/New Delhi Emmes Group: Building a better future for us all Emmes Group is transforming the future of clinical research, bringing the promise of new medical discovery closer within reach for patients Emmes Group was founded as Emmes more than 47 years ago, becoming one of the primary clinical research providers to the US government before expanding into public-private partnerships and commercial biopharma Emmes has built industry leading capabilities in cell and gene therapy, vaccines and infectious diseases, ophthalmology, rare diseases, and neuroscience We believe the work we do will have a direct impact on patients lives and act accordingly We strive to build a collaborative culture at the intersection of being a performance and people driven company We re looking for talented professionals eager to help advance clinical research as we work to embed innovation into the fabric of our company If you share our motivations and passion in research, come join us! Primary Purpose The Application Analyst supports assigned Level 1 or 2 business applications and works with staff to collect information about current business processes to determine impact to the business application Application Analysts may serve as backup or trainee on Level 3 business applications The Application Analyst advises management on best outcomes and will support colleagues from across the company to resolve business process and application issues and put appropriate solutions in place Application Analysts also provide support within initiatives related to assigned business applications Responsibilities Communicate with stakeholders to ensure mutual understanding of requirements and functional specifications Review business processes involving assigned business applications and develop optimization strategies, including gathering critical information from meetings with various stakeholders and producing useful reports Evaluate needs and determination of feasibility based on business application capabilities and process improvement standards Document and effectively communicate your efforts, insights, and recommendations, including conducting meetings and presentations to share ideas and findings Ensure assigned business applications and processes meet business needs and requirements through user acceptance testing Research and propose efficient and economical ways to improve processes and optimize efficiencies within the assigned business applications Develop relationships throughout the company and its affiliates Assist with creation of and update training documents related to assigned business applications Develop skills in multiple technical environments and grasp a variety of business processes Resolve support issues related to assigned business applications Supports adoption efforts and usage optimization related to assigned business applications Assist with development of communications (both in written and in presentation formats) that convey ideas and recommendations in a clear and convincing way related to assigned business applications Build vendor partnerships for assigned applications Provides coaching and training as needed for new or junior team members Assist with release management for assigned applications May serve as technical owner of assigned applications May participate in validation activities as needed Other duties as assigned Qualifications Bachelor s degree in Business or related field with 2+ years of analytical experience Experience in configuring and resolving issues in multiple Veeva Vaults required Exceptional analytical and conceptual thinking skills Ability to influence stakeholders and work closely with them to determine acceptable solutions Excellent communication and documentation skills, including technical writing Experience creating detailed assessments and giving presentations Excellent planning, organization, and time management skills Experience leading and supporting successful projects Experience with strategic business process modeling and traceability CONNECT WITH US! 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Leads project-specific certification activities at the direction of the Manager, OCMPG and Ophthalmic Certification Project Managers Performs certification data entry and works in the certification database at the direction of the Manager, OCMPG and Ophthalmic Certification Project Managers Assists with providing support in tracking, compiling, and submitting project deadlines and deliverables Assists with the collection of electronic and paper-based project files and archives Assists with the review of study related documents, certifications and data to ensure quality and accuracy Supports the coordinating of conference calls and meetings Edits, formats, tracks and distributes technical and non-technical reports Attends and participates in department team meetings Performs other duties as assigned Overview Ophthalmic Certification Project Associate India - Bangalore Emmes Group: Building a better future for us all Emmes Group is transforming the future of clinical research, bringing the promise of new medical discovery closer within reach for patients Emmes Group was founded as Emmes more than 47 years ago, becoming one of the primary clinical research providers to the US government before expanding into public-private partnerships and commercial biopharma Emmes has built industry leading capabilities in cell and gene therapy, vaccines and infectious diseases, ophthalmology, rare diseases, and neuroscience We believe the work we do will have a direct impact on patients lives and act accordingly We stive to build a collaborative culture at the intersection of being a performance and people driven company We re looking for talented professionals eager to help advance clinical research as we work to embed innovation into the fabric of our company If you share our motivations and passion in research, come join us! This requirement is for our OptymEdge division OptymEdge sets the gold standard for training and certification in ophthalmic clinical trials and brings experience and expertise from having the largest and longest-standing certification organization in the industry Pioneering visual acuity certification from conception, we have developed proven solutions for training and certification of Visual Function Examiners and Visual Function Rooms, and partner with study teams to provide visual function certification that ensures a high level of quality and consistency for ophthalmic clinical trial data OptymEdge has certified over 2000 sites worldwide since 1995, working on Phase I through post-marketing trials in clinical Ophthalmology, Optometry, and other therapeutic areas Primary Purpose The Ophthalmic Certification Project Associate (OCPA) is critical to the successful conduct of ophthalmic certifications in Biopharmaceutical-sponsored clinical trials The OCPA supports the Manager, Ophthalmic Certification Project Management Group (OCMPG) and Ophthalmic Certification Project Managers by providing logistical support for electronic document filing and archiving, reporting requirements and other duties required by the statement of work The OCPA will be site-facing through the life cycle of the study, and contributes to team and financial efficiency, work product quality, and client satisfaction through strong relationship management Responsibilities Leads project-specific certification activities at the direction of the Manager, OCMPG and Ophthalmic Certification Project Managers Performs certification data entry and works in the certification database at the direction of the Manager, OCMPG and Ophthalmic Certification Project Managers Assists with providing support in tracking, compiling, and submitting project deadlines and deliverables Assists with the collection of electronic and paper-based project files and archives Assists with the review of study related documents, certifications and data to ensure quality and accuracy Supports the coordinating of conference calls and meetings Edits, formats, tracks and distributes technical and non-technical reports Attends and participates in department team meetings Performs other duties as assigned Qualifications Bachelor s degree preferred or equivalent experience will be considered 2 years demonstrating related experience Demonstrated experience with MS Office Suite, particularly MS Word Time management and decision-making skills Attention to detail and the ability to address several assignments simultaneously Excellent oral and written communication skills Some knowledge of clinical trials in ophthalmology preferred CONNECT WITH US! Follow us on Twitter - @EmmesCRO Find us on LinkedIn - Emmes

Responsible for the day-to-day management and maintenance of the data lake infrastructure, including data ingestion, storage, organization, and retrieval processes. Monitor and assess the quality of data stored in the data lake, identify inconsistencies, errors, and gaps, and collaborate with relevant stakeholders to address data quality issues. Develop and implement data integration and transformation pipelines to ingest, cleanse, and transform data from various sources into the data lake, ensuring compatibility and consistency. Develop and implement data integration and transformation pipelines to ingest, cleanse, and transform data from various sources into the data lake, ensuring compatibility and consistency. Implement and enforce data governance policies and security measures to safeguard sensitive and confidential data stored in the data lake, in compliance with regulatory requirements and best practices. Identify opportunities to optimize the performance and efficiency of the data lake infrastructure, including storage optimization, query performance tuning, and resource utilization monitoring. Conduct exploratory data analysis and perform ad-hoc queries to extract insights and derive actionable intelligence from the data lake, supporting decision-making processes across the organization. Maintain comprehensive documentation of data lake processes, configurations, and workflows, and generate regular reports on data lake performance, usage metrics, and data quality metrics. Collaborate with cross-functional teams, including data engineers, data scientists, business analysts, project managers, and internal/external IT professionals, to understand data requirements, prioritize initiatives, and deliver data solutions that meet business needs. Overview Job Posting Title India Remote/Ahmedabad/Bengaluru/New Delhi Emmes Group: Building a better future for us all. Emmes Group is transforming the future of clinical research, bringing the promise of new medical discovery closer within reach for patients. Emmes Group was founded as Emmes more than 47 years ago, becoming one of the primary clinical research providers to the US government before expanding into public-private partnerships and commercial biopharma. Emmes has built industry leading capabilities in cell and gene therapy, vaccines and infectious diseases, ophthalmology, rare diseases, and neuroscience. We believe the work we do will have a direct impact on patients lives and act accordingly. We strive to build a collaborative culture at the intersection of being a performance and people driven company. We re looking for talented professionals eager to help advance clinical research as we work to embed innovation into the fabric of our company. If you share our motivations and passion in research, come join us! Primary Purpose This position will support and optimize our data lake infrastructure and play a crucial role in ensuring the reliability, efficiency, and usability of our data lake environment Responsibilities Responsible for the day-to-day management and maintenance of the data lake infrastructure, including data ingestion, storage, organization, and retrieval processes. Monitor and assess the quality of data stored in the data lake, identify inconsistencies, errors, and gaps, and collaborate with relevant stakeholders to address data quality issues. Develop and implement data integration and transformation pipelines to ingest, cleanse, and transform data from various sources into the data lake, ensuring compatibility and consistency. Develop and implement data integration and transformation pipelines to ingest, cleanse, and transform data from various sources into the data lake, ensuring compatibility and consistency. Implement and enforce data governance policies and security measures to safeguard sensitive and confidential data stored in the data lake, in compliance with regulatory requirements and best practices. Identify opportunities to optimize the performance and efficiency of the data lake infrastructure, including storage optimization, query performance tuning, and resource utilization monitoring. Conduct exploratory data analysis and perform ad-hoc queries to extract insights and derive actionable intelligence from the data lake, supporting decision-making processes across the organization. Maintain comprehensive documentation of data lake processes, configurations, and workflows, and generate regular reports on data lake performance, usage metrics, and data quality metrics. Collaborate with cross-functional teams, including data engineers, data scientists, business analysts, project managers, and internal/external IT professionals, to understand data requirements, prioritize initiatives, and deliver data solutions that meet business needs. Qualifications Bachelors degree or higher in Computer Science, Information Systems, Statistics, Mathematics, or a related field. Skilled in using Azure specific tools for data analysis, including Microsoft Fabric, Azure Synapse Analytics for big data and complex analysis tasks, and Microsoft Power BI for data visualization and business intelligence solutions. Proficiency in SQL and experience with database management systems (DBMS) for querying, manipulating, and analyzing large datasets. Strong analytical and problem-solving skills, with the ability to interpret complex data sets, identify patterns, and draw meaningful insights. Familiarity with data modeling concepts, data warehousing principles, and ETL (Extract, Transform, Load) processes. Experience with other cloud platforms like AWS and GCP is a plus. Excellent communication and interpersonal skills, with the ability to effectively communicate technical concepts to non-technical stakeholders. Strong attention to detail and a commitment to data accuracy, integrity, and security. CONNECT WITH US! Follow us on Twitter - @EmmesCRO Find us on LinkedIn - Emmes #LI-Remote

JOB_DESCRIPTION.SHARE.HTML CAROUSEL_PARAGRAPH JOB_DESCRIPTION.SHARE.HTML India - Bengaluru Information Technology No Regular Full-Time 2558 Emmes Global mail_outline Get future jobs matching this search or Overview Job Description BI Analyst India: Bengaluru - hybrid Emmes Group: Building a better future for us all. Emmes Group is transforming the future of clinical research, bringing the promise of new medical discovery closer within reach for patients. Emmes Group was founded as Emmes more than 47 years ago, becoming one of the primary clinical research providers to the US government before expanding into public-private partnerships and commercial biopharma. Emmes has built industry leading capabilities in cell and gene therapy, vaccines and infectious diseases, ophthalmology, rare diseases, and neuroscience. We believe the work we do will have a direct impact on patients’ lives and act accordingly. We strive to build a collaborative culture at the intersection of being a performance and people driven company. We’re looking for talented professionals eager to help advance clinical research as we work to embed innovation into the fabric of our company. If you share our motivations and passion in research, come join us! Primary Purpose The Business Intelligence Analyst role requires design and development of interactive dashboards and reports using Amazon QuickSight. Responsibilities include creating calculated fields, building insightful visualizations, and ensuring data accuracy through validation and debugging. This role involves close collaboration with engineers, data scientists, and designers to deliver high-quality, user-centric dashboards that align with business requirements and design standards. Responsibilities Develop interactive dashboards and reports in Amazon QuickSight using pre-configured data sets and schema definitions, ensuring outputs are intuitive and actionable. Create and manage calculated fields and derived metrics from base datasets to support key business questions and performance monitoring. Extend QuickSight capabilities beyond basic usage—leveraging advanced features such as parameters, actions, filters, and embedded visualizations based on documentation and community insights. Collaborate with cross-functional teams including product managers, UX designers, data engineers, software engineers, and clinical operations to ensure dashboards align with user needs and operational goals. Validate and QA dashboards, ensuring that visualizations meet design standards, stakeholder expectations, and data quality benchmarks. Other duties as assigned Qualifications Bachelor’s degree in a quantitative field such as Mathematics, Business, Economics, Engineering, or a related discipline. 4 years of experience working as part of team in a business intelligence analyst or equivalent role. Hands-on experience with leading BI tools such as Tableau, Power BI, or other visualization platforms, with demonstrated ability to build clear, insightful dashboards. Ability to quickly learn new BI tools—this role will require onboarding to Amazon QuickSight. Prior experience in learning new platforms independently using documentation and community resources is a strong plus. Strong analytical skills with the ability to interpret and work with complex data sets, drawing meaningful insights that support business and clinical goals. Exceptional attention to detail to ensure data accuracy, consistency, and integrity across reports and dashboards. Strong visualization quality control mindset, ensuring all visual elements match design mocks, specifications, and stakeholder expectations. Familiarity with clinical trial data or healthcare-related datasets (at least at a high level), including concepts like patient visits, protocol events, and outcomes tracking. CONNECT WITH US! Follow us on Twitter - @EmmesCRO Find us on LinkedIn - Emmes Show more Show less

Develop interactive dashboards and reports in Amazon QuickSight using pre-configured data sets and schema definitions, ensuring outputs are intuitive and actionable Create and manage calculated fields and derived metrics from base datasets to support key business questions and performance monitoring Extend QuickSight capabilities beyond basic usage leveraging advanced features such as parameters, actions, filters, and embedded visualizations based on documentation and community insights Collaborate with cross-functional teams including product managers, UX designers, data engineers, software engineers, and clinical operations to ensure dashboards align with user needs and operational goals Validate and QA dashboards, ensuring that visualizations meet design standards, stakeholder expectations, and data quality benchmarks Other duties as assigned Overview BI Analyst India: Bengaluru - hybrid Emmes Group: Building a better future for us all Emmes Group is transforming the future of clinical research, bringing the promise of new medical discovery closer within reach for patients Emmes Group was founded as Emmes more than 47 years ago, becoming one of the primary clinical research providers to the US government before expanding into public-private partnerships and commercial biopharma Emmes has built industry leading capabilities in cell and gene therapy, vaccines and infectious diseases, ophthalmology, rare diseases, and neuroscience We believe the work we'do will have a direct impact on patients lives and act accordingly We strive to build a collaborative culture at the intersection of being a performance and people driven company we're looking for talented professionals eager to help advance clinical research as we work to embed innovation into the fabric of our company If you share our motivations and passion in research, come join us! Primary Purpose The Business Intelligence Analyst role requires design and development of interactive dashboards and reports using Amazon QuickSight Responsibilities include creating calculated fields, building insightful visualizations, and ensuring data accuracy through validation and debugging This role involves close collaboration with engineers, data scientists, and designers to deliver high-quality, user-centric dashboards that align with business requirements and design standards Responsibilities Develop interactive dashboards and reports in Amazon QuickSight using pre-configured data sets and schema definitions, ensuring outputs are intuitive and actionable Create and manage calculated fields and derived metrics from base datasets to support key business questions and performance monitoring Extend QuickSight capabilities beyond basic usage leveraging advanced features such as parameters, actions, filters, and embedded visualizations based on documentation and community insights Collaborate with cross-functional teams including product managers, UX designers, data engineers, software engineers, and clinical operations to ensure dashboards align with user needs and operational goals Validate and QA dashboards, ensuring that visualizations meet design standards, stakeholder expectations, and data quality benchmarks Other duties as assigned Qualifications bachelors degree in a quantitative field such as Mathematics, Business, Economics, Engineering, or a related discipline 4 years of experience working as part of team in a business intelligence analyst or equivalent role Hands-on experience with leading BI tools such as Tableau, Power BI, or other visualization platforms, with demonstrated ability to build clear, insightful dashboards Ability to quickly learn new BI tools this role will require onboarding to Amazon QuickSight Prior experience in learning new platforms independently using documentation and community resources is a strong plus Strong analytical skills with the ability to interpret and work with complex data sets, drawing meaningful insights that support business and clinical goals Exceptional attention to detail to ensure data accuracy, consistency, and integrity across reports and dashboards Strong visualization quality control mindset, ensuring all visual elements match design mocks, specifications, and stakeholder expectations Familiarity with clinical trial data or healthcare-related datasets (at least at a high level), including concepts like patient visits, protocol events, and outcomes tracking

JOB_DESCRIPTION.SHARE.HTML CAROUSEL_PARAGRAPH JOB_DESCRIPTION.SHARE.HTML India - Bengaluru Project / Program Management No Regular Full-Time 2554 Emmes Global mail_outline Get future jobs matching this search or Overview Job Description Project Specialist India Bengaluru - hybrid Emmes Group: Building a better future for us all. Emmes Group is transforming the future of clinical research, bringing the promise of new medical discovery closer within reach for patients. Emmes Group was founded as Emmes more than 47 years ago, becoming one of the primary clinical research providers to the US government before expanding into public-private partnerships and commercial biopharma. Emmes has built industry leading capabilities in cell and gene therapy, vaccines and infectious diseases, ophthalmology, rare diseases, and neuroscience. We believe the work we do will have a direct impact on patients’ lives and act accordingly. We strive to build a collaborative culture at the intersection of being a performance and people driven company. We’re looking for talented professionals eager to help advance clinical research as we work to embed innovation into the fabric of our company. If you share our motivations and passion in research, come join us! Primary Purpose The Project Specialist provides support to Emmes Global Project Management teams, determining workflows, providing logistics support for conference calls, meetings, supplies, documentation, problem solving, and client/sponsor reporting needs and interactions as required by the statement of work or other corporate/client/sponsor requirements. This role supports BioPharma portfolio projects. Responsibilities Supports Global Project Manager (GPM) responsibilities to ensure the contracted services are in accordance with the executed contract and Client/Study expectations. Acts as a secondary point of contact in with study vendor(s). Supports vendor management to ensure effective oversight of third-party vendors. Assists in contributing to project milestone tracking and schedule management. Supports GPM in project resource requests and study FTE allocation and tracking. Supports GPM in risk management activities. Schedules and attends internal and external team meetings. May lead and/or assist GPM in internal team meetings and portions of external team meetings as applicable. Supports agenda preparation and prepares and distributes meeting minutes for internal and external meetings. Assists GPM in facilitating communication between staff and client regarding project development and project processes. Extracts information from designated clinical trial management system (CTMS) and other systems/tools to track/analyze study progress for the GPM (e.g., regulatory documents, enrollment, SAE/AEs, protocol deviations, supplies, ethics approvals, data queries) along with coordinating and drafting status reports for internal and external stakeholders. Supports project administrative activities for internal and external audits. Assists in overseeing TMF activities to ensure the TMF is maintained in inspection ready state. Tasks include but are not limited to: tracking of quality and status of document filing, timeliness of document filing, collaborating with TMF group to ensure contemporaneous TMF maintenance. Assists the GPM with project financial management activities including monthly projections and budget tracking. Assists in the development of study documents and plans, using project-specific knowledge. Establishes and maintains procedures and processes (e.g., SOPs, work practices) in conjunction with departments and broader Company. May also contribute to corporate SOP development, Assists with periodic review of allocated project specific internal business records and associated project TMF. Serves as administrator of shared workspace and Emmes Systems for assigned projects. Assists with onboarding, offboarding, and training records for project staff. Assists in managing document retention and archive of project. Performs other duties as assigned. Qualifications Bachelor’s Degree or equivalent qualification. Minimum 4 years of relevant project or administrative support experience. Required Skills/Abilities Strong familiarity and working knowledge of Microsoft Office applications, particularly MS Word, Excel, SharePoint, Teams and Emmes systems. \ Strong analytical skills. Must be able to organize and manage workload efficiently and prioritize projects with minimal supervision. Must be able to work with minimal supervision to perform work that is varied and should be able to work to tight timelines. CONNECT WITH US! Follow us on Twitter - @EmmesCRO Find us on LinkedIn - Emmes Show more Show less

Supports Global Project Manager (GPM) responsibilities to ensure the contracted services are in accordance with the executed contract and Client/Study expectations Acts as a secondary point of contact in with study vendor(s) Supports vendor management to ensure effective oversight of third-party vendors Contributes to project milestone tracking and schedule management \ Supports GPM in project resource requests and study FTE allocation and tracking Supports GPM in risk management activities Schedules and attends internal and external team meetings Leads and/or assists GPM in internal team meetings and portions of external team meetings as applicable Supports agenda preparation and prepares and distributes meeting minutes for internal and external meetings \ Assists GPM in Facilitating communication between staff and client regarding project development and project processes Extracts information from designated clinical trial management system (CTMS) and other systems/tools to track/analyze study progress for the GPM (e g , regulatory documents, enrollment, SAE/AEs, protocol deviations, supplies, ethics approvals, data queries) along with coordinating and drafting status reports for internal and external stakeholders Supports project administrative activities for internal and external audits Oversees TMF activities to ensure the TMF is maintained in inspection ready state Tasks include but are not limited to: tracking of quality and status of document filing, timeliness of document filing, collaborate with TMF group to ensure contemporaneous TMF maintenance Assists the GPM with project financial management activities including monthly projections and budget tracking Develops study documents and plans, using project-specific knowledge Establishes and maintains procedures and processes (e g , SOPs, work practices) in conjunction with departments and broader Company May also contribute to corporate SOP development Performs periodic review of allocated project specific internal business records and associated project TMF as needed Serves as administrator of shared workspace and Emmes Systems for assigned projects Assists with onboarding, offboarding, and training records for project staff Manages document retention and archive of project Provides oversight of Project Specialists and Clinical Project Coordinators Performs other duties as assigned Overview Sr Project Specialist India Bengaluru/hybrid Emmes Group: Building a better future for us all Emmes Group is transforming the future of clinical research, bringing the promise of new medical discovery closer within reach for patients Emmes Group was founded as Emmes more than 47 years ago, becoming one of the primary clinical research providers to the US government before expanding into public-private partnerships and commercial biopharma Emmes has built industry leading capabilities in cell and gene therapy, vaccines and infectious diseases, ophthalmology, rare diseases, and neuroscience We believe the work we do will have a direct impact on patients lives and act accordingly We strive to build a collaborative culture at the intersection of being a performance and people driven company We re looking for talented professionals eager to help advance clinical research as we work to embed innovation into the fabric of our company If you share our motivations and passion in research, come join us! Primary Purpose The Senior Project Specialist provides support to Emmes Global Project Management teams, determining workflows, providing logistics support for conference calls, meetings, supplies, documentation, problem solving, and client/sponsor reporting needs and interactions as required by the statement of work or other corporate/client/sponsor requirements This position provides oversight to Project Specialists and Clinical Project Coordinators This role supports BioPharma portfolio projects Responsibilities Supports Global Project Manager (GPM) responsibilities to ensure the contracted services are in accordance with the executed contract and Client/Study expectations Acts as a secondary point of contact in with study vendor(s) Supports vendor management to ensure effective oversight of third-party vendors Contributes to project milestone tracking and schedule management \ Supports GPM in project resource requests and study FTE allocation and tracking Supports GPM in risk management activities Schedules and attends internal and external team meetings Leads and/or assists GPM in internal team meetings and portions of external team meetings as applicable Supports agenda preparation and prepares and distributes meeting minutes for internal and external meetings \ Assists GPM in Facilitating communication between staff and client regarding project development and project processes Extracts information from designated clinical trial management system (CTMS) and other systems/tools to track/analyze study progress for the GPM (e g , regulatory documents, enrollment, SAE/AEs, protocol deviations, supplies, ethics approvals, data queries) along with coordinating and drafting status reports for internal and external stakeholders Supports project administrative activities for internal and external audits Oversees TMF activities to ensure the TMF is maintained in inspection ready state Tasks include but are not limited to: tracking of quality and status of document filing, timeliness of document filing, collaborate with TMF group to ensure contemporaneous TMF maintenance Assists the GPM with project financial management activities including monthly projections and budget tracking Develops study documents and plans, using project-specific knowledge Establishes and maintains procedures and processes (e g , SOPs, work practices) in conjunction with departments and broader Company May also contribute to corporate SOP development Performs periodic review of allocated project specific internal business records and associated project TMF as needed Serves as administrator of shared workspace and Emmes Systems for assigned projects Assists with onboarding, offboarding, and training records for project staff Manages document retention and archive of project Provides oversight of Project Specialists and Clinical Project Coordinators Performs other duties as assigned Qualifications Bachelor s Degree or equivalent qualification Minimum 6 years of relevant project or administrative support experience Required Skills/Abilities Strong familiarity and working knowledge of Microsoft Office applications, particularly MS Word, Excel, SharePoint, Teams and Emmes systems Strong analytical skills Must be able to organize and manage workload efficiently and prioritize projects with minimal supervision Must be able to work with minimal supervision to perform work that is varied and should be able to work to tight timelines CONNECT WITH US! Follow us on Twitter - @EmmesCRO Find us on LinkedIn - Emmes #LI

Supports Global Project Manager (GPM) responsibilities to ensure the contracted services are in accordance with the executed contract and Client/Study expectations Acts as a secondary point of contact in with study vendor(s) Supports vendor management to ensure effective oversight of third-party vendors Assists in contributing to project milestone tracking and schedule management Supports GPM in project resource requests and study FTE allocation and tracking Supports GPM in risk management activities Schedules and attends internal and external team meetings May lead and/or assist GPM in internal team meetings and portions of external team meetings as applicable Supports agenda preparation and prepares and distributes meeting minutes for internal and external meetings Assists GPM in facilitating communication between staff and client regarding project development and project processes Extracts information from designated clinical trial management system (CTMS) and other systems/tools to track/analyze study progress for the GPM (e g , regulatory documents, enrollment, SAE/AEs, protocol deviations, supplies, ethics approvals, data queries) along with coordinating and drafting status reports for internal and external stakeholders Supports project administrative activities for internal and external audits Assists in overseeing TMF activities to ensure the TMF is maintained in inspection ready state Tasks include but are not limited to: tracking of quality and status of document filing, timeliness of document filing, collaborating with TMF group to ensure contemporaneous TMF maintenance Assists the GPM with project financial management activities including monthly projections and budget tracking Assists in the development of study documents and plans, using project-specific knowledge Establishes and maintains procedures and processes (e g , SOPs, work practices) in conjunction with departments and broader Company May also contribute to corporate SOP development, Assists with periodic review of allocated project specific internal business records and associated project TMF Serves as administrator of shared workspace and Emmes Systems for assigned projects Assists with onboarding, offboarding, and training records for project staff Assists in managing document retention and archive of project Performs other duties as assigned Overview Project Specialist India Bengaluru - hybrid Emmes Group: Building a better future for us all Emmes Group is transforming the future of clinical research, bringing the promise of new medical discovery closer within reach for patients Emmes Group was founded as Emmes more than 47 years ago, becoming one of the primary clinical research providers to the US government before expanding into public-private partnerships and commercial biopharma Emmes has built industry leading capabilities in cell and gene therapy, vaccines and infectious diseases, ophthalmology, rare diseases, and neuroscience We believe the work we do will have a direct impact on patients lives and act accordingly We strive to build a collaborative culture at the intersection of being a performance and people driven company We re looking for talented professionals eager to help advance clinical research as we work to embed innovation into the fabric of our company If you share our motivations and passion in research, come join us! Primary Purpose The Project Specialist provides support to Emmes Global Project Management teams, determining workflows, providing logistics support for conference calls, meetings, supplies, documentation, problem solving, and client/sponsor reporting needs and interactions as required by the statement of work or other corporate/client/sponsor requirements This role supports BioPharma portfolio projects Responsibilities Supports Global Project Manager (GPM) responsibilities to ensure the contracted services are in accordance with the executed contract and Client/Study expectations Acts as a secondary point of contact in with study vendor(s) Supports vendor management to ensure effective oversight of third-party vendors Assists in contributing to project milestone tracking and schedule management Supports GPM in project resource requests and study FTE allocation and tracking Supports GPM in risk management activities Schedules and attends internal and external team meetings May lead and/or assist GPM in internal team meetings and portions of external team meetings as applicable Supports agenda preparation and prepares and distributes meeting minutes for internal and external meetings Assists GPM in facilitating communication between staff and client regarding project development and project processes Extracts information from designated clinical trial management system (CTMS) and other systems/tools to track/analyze study progress for the GPM (e g , regulatory documents, enrollment, SAE/AEs, protocol deviations, supplies, ethics approvals, data queries) along with coordinating and drafting status reports for internal and external stakeholders Supports project administrative activities for internal and external audits Assists in overseeing TMF activities to ensure the TMF is maintained in inspection ready state Tasks include but are not limited to: tracking of quality and status of document filing, timeliness of document filing, collaborating with TMF group to ensure contemporaneous TMF maintenance Assists the GPM with project financial management activities including monthly projections and budget tracking Assists in the development of study documents and plans, using project-specific knowledge Establishes and maintains procedures and processes (e g , SOPs, work practices) in conjunction with departments and broader Company May also contribute to corporate SOP development, Assists with periodic review of allocated project specific internal business records and associated project TMF Serves as administrator of shared workspace and Emmes Systems for assigned projects Assists with onboarding, offboarding, and training records for project staff Assists in managing document retention and archive of project Performs other duties as assigned Qualifications Bachelor s Degree or equivalent qualification Minimum 4 years of relevant project or administrative support experience Required Skills/Abilities Strong familiarity and working knowledge of Microsoft Office applications, particularly MS Word, Excel, SharePoint, Teams and Emmes systems \ Strong analytical skills Must be able to organize and manage workload efficiently and prioritize projects with minimal supervision Must be able to work with minimal supervision to perform work that is varied and should be able to work to tight timelines CONNECT WITH US! Follow us on Twitter - @EmmesCRO Find us on LinkedIn - Emmes #LI

JOB_DESCRIPTION.SHARE.HTML CAROUSEL_PARAGRAPH JOB_DESCRIPTION.SHARE.HTML India - Bengaluru Information Technology No Regular Full-Time 2512 Emmes Global mail_outline Get future jobs matching this search or Overview Job Description Job Posting Title India Remote/Ahmedabad/Bengaluru/New Delhi Emmes Group: Building a better future for us all. Emmes Group is transforming the future of clinical research, bringing the promise of new medical discovery closer within reach for patients. Emmes Group was founded as Emmes more than 47 years ago, becoming one of the primary clinical research providers to the US government before expanding into public-private partnerships and commercial biopharma. Emmes has built industry leading capabilities in cell and gene therapy, vaccines and infectious diseases, ophthalmology, rare diseases, and neuroscience. We believe the work we do will have a direct impact on patients’ lives and act accordingly. We strive to build a collaborative culture at the intersection of being a performance and people driven company. We’re looking for talented professionals eager to help advance clinical research as we work to embed innovation into the fabric of our company. If you share our motivations and passion in research, come join us! Responsibilities Primary Purpose Qualifications CONNECT WITH US! Follow us on Twitter - @EmmesCRO Find us on LinkedIn - Emmes

Designs, develops, and enhances Android Native Mobile app used in clinical trials. Collaborate closely with Product Owners, UI/UX designers, backend developers, and QA teams to translate business requirements into technical solutions. Adheres to best practices and Emmes quality standards for code security, optimization, and reusability. Uses established frameworks for a seamless user experience across platforms. Performs unit testing, debugging, and troubleshooting as needed to ensure quality of work. Performs code reviews, assesses regression impact for design changes, and completes technical documentation. Identifies opportunities for refactoring/reworking major modules and sees implementation through to deployment. Ensure mobile applications are compatible with the latest Android versions and devices. Mentors junior team members. Overview Job Posting Title India Remote/Ahmedabad/Bengaluru/New Delhi Emmes Group: Building a better future for us all. Emmes Group is transforming the future of clinical research, bringing the promise of new medical discovery closer within reach for patients. Emmes Group was founded as Emmes more than 47 years ago, becoming one of the primary clinical research providers to the US government before expanding into public-private partnerships and commercial biopharma. Emmes has built industry leading capabilities in cell and gene therapy, vaccines and infectious diseases, ophthalmology, rare diseases, and neuroscience. We believe the work we do will have a direct impact on patients lives and act accordingly. We strive to build a collaborative culture at the intersection of being a performance and people driven company. We re looking for talented professionals eager to help advance clinical research as we work to embed innovation into the fabric of our company. If you share our motivations and passion in research, come join us! Primary Purpose Designs, develops, and enhances cloud-based, software-as-a-service (SaaS) web-based clinical trials applications. Responsibilities Designs, develops, and enhances Android Native Mobile app used in clinical trials. Collaborate closely with Product Owners, UI/UX designers, backend developers, and QA teams to translate business requirements into technical solutions. Adheres to best practices and Emmes quality standards for code security, optimization, and reusability. Uses established frameworks for a seamless user experience across platforms. Performs unit testing, debugging, and troubleshooting as needed to ensure quality of work. Performs code reviews, assesses regression impact for design changes, and completes technical documentation. Identifies opportunities for refactoring/reworking major modules and sees implementation through to deployment. Ensure mobile applications are compatible with the latest Android versions and devices. Mentors junior team members. Qualifications 6 or more years of related professional experience. Any of the following additional technical skills would be a plus: Expertise with iOS development Experience with Material Design Experience with Material-UI or other front-end libraries Required Education: B.E/MTech/MCA degree in a computer related field. Note: Satisfactory background check required. CONNECT WITH US! Follow us on Twitter - @EmmesCRO Find us on LinkedIn - Emmes #LI

Manages overall initiative lifecycle, including the day-to-day activities of planning, coordinating, implementing, monitoring, documenting, and completing assigned initiatives across global teams Monitors initiatives to ensure initiative framework processes are being followed and project management best practices are being used, including reporting on metrics related to initiative health, completion of milestones on time and within budget, and adoption of effective change management processes Coordinates tasks and communication within and across teams and develops presentation materials for projects and executives Partners with business leaders to ensure alignment of initiative scope and deliverables with business and corporate strategies Facilitates or leads initiative meetings to develop efficient and effective future state outcome and to identify deliverables needed to ensure initiative goals are met Works with Business Analyst Manager to develop an effective change management plan for assigned initiatives, then serves as the change agent champion and lead the execution of the change management plan Compiles and provides monthly initiative status reports, KPIs and metrics related to health of assigned initiatives to executive sponsors, stakeholders, and peers, including key updates, cost, schedule, status, and risks Exercises independent discretion and judgment to solve complex problems regarding project, department, or division-related work Promotes, develops, and maintains disciplined initiative project management models and frameworks (and related tools and processes) across Emmes and its subsidiaries; ensures adherence, adoption, implementation, and review of lessons learned Initiates and shares learning opportunities for the initiative team to continue to grow as professionals Coordinates activities with Business Analyst and/or Application Analyst assigned to initiative Assists with tracking project expenditure Provides training, coaching, and mentoring to junior team members Provides management to direct reports and leadership to full team Manages vendor relationships during vendor-run implementations Performs other duties as assigned Overview Emmes Group: Building a better future for us all Emmes Group is transforming the future of clinical research, bringing the promise of new medical discovery closer within reach for patients Emmes Group was founded as Emmes more than 47 years ago, becoming one of the primary clinical research providers to the US government before expanding into public-private partnerships and commercial biopharma Emmes has built industry leading capabilities in cell and gene therapy, vaccines and infectious diseases, ophthalmology, rare diseases, and neuroscience We believe the work we do will have a direct impact on patients lives and act accordingly We strive to build a collaborative culture at the intersection of being a performance and people driven company We re looking for talented professionals eager to help advance clinical research as we work to embed innovation into the fabric of our company If you share our motivations and passion in research, come join us! Primary Purpose The Senior Project Manager, Initiatives is responsible for the project life cycle for various organizational initiatives, some of which are listed in the Emmes Strategic Scorecard This position works closely with members of the Executive and Operations Team, who serve as Executive Sponsors of initiatives This position is expected to hold information confidential and act as a trusted confidant of Executives The Senior Project Manager, Initiatives will manage all aspects of assigned initiatives of varying complexity and medium to large size by assembling work groups, assigning individual responsibilities, identifying needed resources, developing schedules to ensure timely project completion, identifying critical capabilities, project resources, budgets, risks and critical path issues As the senior member of the team, this position provides training, coaching and mentoring to junior team members, and manages direct reports Responsibilities Manages overall initiative lifecycle, including the day-to-day activities of planning, coordinating, implementing, monitoring, documenting, and completing assigned initiatives across global teams Monitors initiatives to ensure initiative framework processes are being followed and project management best practices are being used, including reporting on metrics related to initiative health, completion of milestones on time and within budget, and adoption of effective change management processes Coordinates tasks and communication within and across teams and develops presentation materials for projects and executives Partners with business leaders to ensure alignment of initiative scope and deliverables with business and corporate strategies Facilitates or leads initiative meetings to develop efficient and effective future state outcome and to identify deliverables needed to ensure initiative goals are met Works with Business Analyst Manager to develop an effective change management plan for assigned initiatives, then serves as the change agent champion and lead the execution of the change management plan Compiles and provides monthly initiative status reports, KPIs and metrics related to health of assigned initiatives to executive sponsors, stakeholders, and peers, including key updates, cost, schedule, status, and risks Exercises independent discretion and judgment to solve complex problems regarding project, department, or division-related work Promotes, develops, and maintains disciplined initiative project management models and frameworks (and related tools and processes) across Emmes and its subsidiaries; ensures adherence, adoption, implementation, and review of lessons learned Initiates and shares learning opportunities for the initiative team to continue to grow as professionals Coordinates activities with Business Analyst and/or Application Analyst assigned to initiative Assists with tracking project expenditure Provides training, coaching, and mentoring to junior team members Provides management to direct reports and leadership to full team Manages vendor relationships during vendor-run implementations Performs other duties as assigned Qualifications Undergraduate degree in business or humanities field preferred 10+ years of project/program/portfolio management experience with demonstrated increase in responsibility and project complexity, including managing enterprise level business and technology transformation projects as well as resource management, financial management, and/or budget analysis PMP or equivalent certification and a proven track record of successfully managing projects in a fast-paced business Experience building customer and stakeholder relationships with a focus on problem resolution Experience explaining technical terms to non-technical staff Exceptional project management skills with ability to multitask and manage multiple projects across diverse global teams in a highly matrixed environment Demonstrated planning and project management skills Excellent listening, communication, presentation, interpersonal skills, both written and verbal, with an ability to inform, influence, convince and persuade Strong skills in prioritization, organization, decision-making, time management, and planning Ability to drive to tangible results in a timely manner even when the work involves a highlevel of ambiguity Skilled in facilitating meetings with multiple stakeholders, including building consensus, motivation, and managing conflict Strong analytical, problem-solving, and troubleshooting skills; with the ability to collect, organize, analyze, and disseminate significant amounts of information with attention to detail and accuracy Ability to demonstrate strategic thinking capability, exercise good judgement, make sound decisions, and escalate issues/decision making as appropriate Knowledge of technology concepts including Software Development Life Cycle (SDLC), process improvement, and agile methodologies is preferred Experience in O365, Smartsheet or MS Project, and Jira is preferred CONNECT WITH US! Follow us on Twitter - @EmmesCRO Find us on LinkedIn - Emmes #LI

JOB_DESCRIPTION.SHARE.HTML CAROUSEL_PARAGRAPH JOB_DESCRIPTION.SHARE.HTML India - Bengaluru Project / Program Management No Regular Full-Time 2588 Emmes Global mail_outline Get future jobs matching this search or Overview Job Description Emmes Group: Building a better future for us all. Emmes Group is transforming the future of clinical research, bringing the promise of new medical discovery closer within reach for patients. Emmes Group was founded as Emmes more than 47 years ago, becoming one of the primary clinical research providers to the US government before expanding into public-private partnerships and commercial biopharma. Emmes has built industry leading capabilities in cell and gene therapy, vaccines and infectious diseases, ophthalmology, rare diseases, and neuroscience. We believe the work we do will have a direct impact on patients’ lives and act accordingly. We strive to build a collaborative culture at the intersection of being a performance and people driven company. We’re looking for talented professionals eager to help advance clinical research as we work to embed innovation into the fabric of our company. If you share our motivations and passion in research, come join us! Primary Purpose The Senior Project Manager, Initiatives is responsible for the project life cycle for various organizational initiatives, some of which are listed in the Emmes Strategic Scorecard. This position works closely with members of the Executive and Operations Team, who serve as Executive Sponsors of initiatives. This position is expected to hold information confidential and act as a trusted confidant of Executives. The Senior Project Manager, Initiatives will manage all aspects of assigned initiatives of varying complexity and medium to large size by assembling work groups, assigning individual responsibilities, identifying needed resources, developing schedules to ensure timely project completion, identifying critical capabilities, project resources, budgets, risks and critical path issues. As the senior member of the team, this position provides training, coaching and mentoring to junior team members, and manages direct reports Responsibilities Manages overall initiative lifecycle, including the day-to-day activities of planning, coordinating, implementing, monitoring, documenting, and completing assigned initiatives across global teams. Monitors initiatives to ensure initiative framework processes are being followed and project management best practices are being used, including reporting on metrics related to initiative health, completion of milestones on time and within budget, and adoption of effective change management processes. Coordinates tasks and communication within and across teams and develops presentation materials for projects and executives. Partners with business leaders to ensure alignment of initiative scope and deliverables with business and corporate strategies. Facilitates or leads initiative meetings to develop efficient and effective future state outcome and to identify deliverables needed to ensure initiative goals are met. Works with Business Analyst Manager to develop an effective change management plan for assigned initiatives, then serves as the change agent champion and lead the execution of the change management plan. Compiles and provides monthly initiative status reports, KPIs and metrics related to health of assigned initiatives to executive sponsors, stakeholders, and peers, including key updates, cost, schedule, status, and risks. Exercises independent discretion and judgment to solve complex problems regarding project, department, or division-related work. Promotes, develops, and maintains disciplined initiative project management models and frameworks (and related tools and processes) across Emmes and its subsidiaries; ensures adherence, adoption, implementation, and review of lessons learned. Initiates and shares learning opportunities for the initiative team to continue to grow as professionals. Coordinates activities with Business Analyst and/or Application Analyst assigned to initiative. Assists with tracking project expenditure. Provides training, coaching, and mentoring to junior team members. Provides management to direct reports and leadership to full team. Manages vendor relationships during vendor-run implementations. Performs other duties as assigned. Qualifications Undergraduate degree in business or humanities field preferred. 10+ years of project/program/portfolio management experience with demonstrated increase in responsibility and project complexity, including managing enterprise level business and technology transformation projects as well as resource management, financial management, and/or budget analysis. PMP or equivalent certification and a proven track record of successfully managing projects in a fast-paced business. Experience building customer and stakeholder relationships with a focus on problem resolution. Experience explaining technical terms to non-technical staff. Exceptional project management skills with ability to multitask and manage multiple projects across diverse global teams in a highly matrixed environment. Demonstrated planning and project management skills. Excellent listening, communication, presentation, interpersonal skills, both written and verbal, with an ability to inform, influence, convince and persuade. Strong skills in prioritization, organization, decision-making, time management, and planning. Ability to drive to tangible results in a timely manner even when the work involves a highlevel of ambiguity. Skilled in facilitating meetings with multiple stakeholders, including building consensus, motivation, and managing conflict. Strong analytical, problem-solving, and troubleshooting skills; with the ability to collect, organize, analyze, and disseminate significant amounts of information with attention to detail and accuracy. Ability to demonstrate strategic thinking capability, exercise good judgement, make sound decisions, and escalate issues/decision making as appropriate. Knowledge of technology concepts including Software Development Life Cycle (SDLC), process improvement, and agile methodologies is preferred. Experience in O365, Smartsheet or MS Project, and Jira is preferred. CONNECT WITH US! Follow us on Twitter - @EmmesCRO Find us on LinkedIn - Emmes

JOB_DESCRIPTION.SHARE.HTML CAROUSEL_PARAGRAPH JOB_DESCRIPTION.SHARE.HTML India - Bengaluru Project / Program Management No Regular Full-Time 2555 Emmes Global mail_outline Get future jobs matching this search or Overview Job Description Sr Project Specialist India Bengaluru/hybrid Emmes Group: Building a better future for us all. Emmes Group is transforming the future of clinical research, bringing the promise of new medical discovery closer within reach for patients. Emmes Group was founded as Emmes more than 47 years ago, becoming one of the primary clinical research providers to the US government before expanding into public-private partnerships and commercial biopharma. Emmes has built industry leading capabilities in cell and gene therapy, vaccines and infectious diseases, ophthalmology, rare diseases, and neuroscience. We believe the work we do will have a direct impact on patients’ lives and act accordingly. We strive to build a collaborative culture at the intersection of being a performance and people driven company. We’re looking for talented professionals eager to help advance clinical research as we work to embed innovation into the fabric of our company. If you share our motivations and passion in research, come join us! Primary Purpose The Senior Project Specialist provides support to Emmes Global Project Management teams, determining workflows, providing logistics support for conference calls, meetings, supplies, documentation, problem solving, and client/sponsor reporting needs and interactions as required by the statement of work or other corporate/client/sponsor requirements. This position provides oversight to Project Specialists and Clinical Project Coordinators. This role supports BioPharma portfolio projects Responsibilities Supports Global Project Manager (GPM) responsibilities to ensure the contracted services are in accordance with the executed contract and Client/Study expectations. Acts as a secondary point of contact in with study vendor(s). Supports vendor management to ensure effective oversight of third-party vendors. Contributes to project milestone tracking and schedule management. \ Supports GPM in project resource requests and study FTE allocation and tracking. Supports GPM in risk management activities. Schedules and attends internal and external team meetings. Leads and/or assists GPM in internal team meetings and portions of external team meetings as applicable. Supports agenda preparation and prepares and distributes meeting minutes for internal and external meetings. \ Assists GPM in Facilitating communication between staff and client regarding project development and project processes. Extracts information from designated clinical trial management system (CTMS) and other systems/tools to track/analyze study progress for the GPM (e.g., regulatory documents, enrollment, SAE/AEs, protocol deviations, supplies, ethics approvals, data queries) along with coordinating and drafting status reports for internal and external stakeholders. Supports project administrative activities for internal and external audits. Oversees TMF activities to ensure the TMF is maintained in inspection ready state. Tasks include but are not limited to: tracking of quality and status of document filing, timeliness of document filing, collaborate with TMF group to ensure contemporaneous TMF maintenance. Assists the GPM with project financial management activities including monthly projections and budget tracking. Develops study documents and plans, using project-specific knowledge. Establishes and maintains procedures and processes (e.g., SOPs, work practices) in conjunction with departments and broader Company. May also contribute to corporate SOP development. Performs periodic review of allocated project specific internal business records and associated project TMF as needed. Serves as administrator of shared workspace and Emmes Systems for assigned projects. Assists with onboarding, offboarding, and training records for project staff. Manages document retention and archive of project. Provides oversight of Project Specialists and Clinical Project Coordinators. Performs other duties as assigned. Qualifications Bachelor’s Degree or equivalent qualification. Minimum 6 years of relevant project or administrative support experience. Required Skills/Abilities Strong familiarity and working knowledge of Microsoft Office applications, particularly MS Word, Excel, SharePoint, Teams and Emmes systems. Strong analytical skills. Must be able to organize and manage workload efficiently and prioritize projects with minimal supervision. Must be able to work with minimal supervision to perform work that is varied and should be able to work to tight timelines. CONNECT WITH US! Follow us on Twitter - @EmmesCRO Find us on LinkedIn - Emmes