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
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 We’re seeking a creative and motivated Social Media/ Digital Marketing Intern based in India to support our global brand presence on LinkedIn, and other channels. This is an exciting opportunity to gain hands-on experience with content creation, campaign execution, and digital storytelling in the life sciences space. Responsibilities: Assist in the planning, creation, and scheduling of social media content across multiple brand pages (Emmes Group, Emmes, OptymEdge, VaxTrials, Veridix). Design eye-catching graphics, carousels, infographics, and short videos aligned with brand guidelines. Draft engaging copy and CTAs for posts, ensuring alignment with tone and brand messaging Support live event coverage (e.g., conferences, webinars) with social posts and visuals. Monitor social media channels for engagement, comments, and messages, and coordinate the response with marketing team. Conduct competitor research to identify trends and engagement opportunities. Monitor analytics and prepare simple performance reports to track engagement and reach. Optimize post copy and hashtags for maximum visibility and searchability . Support the marketing team with other ad hoc digital activities. Qualifications: Currently pursuing or recently completed a degree in Marketing, Communications, Design, Media, or a related field. Strong knowledge of social media platforms (especially LinkedIn). Graphic design ability required : Proficiency in Canva (required). Basic video editing skills (short reels, animations, motion graphics) desirable. Excellent writing, communication, and organizational skills. Interest in healthcare, life sciences, or technology industries preferred. Self-motivated, detail-oriented, and able to work independently across time zones. CONNECT WITH US! Follow us on Twitter - @EmmesCRO Find us on LinkedIn - Emmes
Overview: A Biostatistician Intern is responsible for working closely with biostatisticians and other clinical research team members on biomedical research projects across a variety of therapeutic areas. The Biostatistics Intern assists on all activities related to the design and development of study protocols, conducting statistical analysis and reporting study outcomes of clinical trials in accordance with the project requirements under the oversight of senior team members. Responsibilities: Prepare statistical study documents (e.g., Statistical analysis plan, randomization plans, statistical programming plan etc.) under oversight of senior team member Performs statistical analysis and prepare summary reports and visualizations including programming Performs Quality Control (QC) for statistical deliverables prepared by independently or by other staff Executes assigned tasks with high quality and integrity Provides accurate, effective and timely communication of issues to senior members of the team. Assists in the development of clinical study report or clinical manuscript through statistical interpretation of study results. Works effectively and collaboratively within biostatistics team Qualifications: Masters/PhD in statistics or biostatistics Familiarity with SAS (mandatory) and R (Optional). Expertise in statistical methods and its applications in Clinical Research Good communication skills Ability to manage priorities effectively Attention to detail Excellent analytical/problem solving skills
Overview: The Statistical Programming Intern provides robust statistical programming support for multiple clinical projects using SAS to deliver key regulatory-compliant outputs. Key responsibilities include developing programming documentation, writing efficient code, and staying updated on statistical programming techniques. This role also provides study updates to study lead while performing assigned duties. Responsibilities: Provides statistical programming support for multiple clinical research study projects or study teams under oversight of lead programmer. Supports key deliverables based on regulatory requirements for clinical research e-submissions and/or study requirements for Sponsor, Regulatory, Investigator or Safety review meetings Supports development of programming documentation and annotations including specifications, adhering to relevant Standard Operating Procedures. Provides accurate, effective and timely communication of issues and status to study lead of the team. Executes assigned tasks with high quality and integrity Works effectively and collaboratively with cross functional teams Qualifications: A bachelor's or master’s degree in science with 0-6 months Statistical programming experience in CDISC/TLF Familiarity with SAS (mandatory) and R (Optional). Ability to prioritize, problem-solve, organize, and make decisions. Good communication skills Attention to detail Excellent analytical/problem solving skills
Overview: The Statistical Programming Intern provides robust statistical programming support for multiple clinical projects using SAS to deliver key regulatory-compliant outputs. Key responsibilities include developing programming documentation, writing efficient code, and staying updated on statistical programming techniques. This role also provides study updates to study lead while performing assigned duties. Responsibilities: Provides statistical programming support for multiple clinical research study projects or study teams under oversight of lead programmer. Supports key deliverables based on regulatory requirements for clinical research e-submissions and/or study requirements for Sponsor, Regulatory, Investigator or Safety review meetings Supports development of programming documentation and annotations including specifications, adhering to relevant Standard Operating Procedures. Provides accurate, effective and timely communication of issues and status to study lead of the team. Executes assigned tasks with high quality and integrity Works effectively and collaboratively with cross functional teams Qualifications: A bachelor's or master’s degree in science with 0-6 months Statistical programming experience in CDISC/TLF Familiarity with SAS (mandatory) and R (Optional). Ability to prioritize, problem-solve, organize, and make decisions. Good communication skills Attention to detail Excellent analytical/problem solving skills
Overview: A Biostatistician Intern is responsible for working closely with biostatisticians and other clinical research team members on biomedical research projects across a variety of therapeutic areas. The Biostatistics Intern assists on all activities related to the design and development of study protocols, conducting statistical analysis and reporting study outcomes of clinical trials in accordance with the project requirements under the oversight of senior team members. Responsibilities: Prepare statistical study documents (e.g., Statistical analysis plan, randomization plans, statistical programming plan etc.) under oversight of senior team member Performs statistical analysis and prepare summary reports and visualizations including programming Performs Quality Control (QC) for statistical deliverables prepared by independently or by other staff Executes assigned tasks with high quality and integrity Provides accurate, effective and timely communication of issues to senior members of the team. Assists in the development of clinical study report or clinical manuscript through statistical interpretation of study results. Works effectively and collaboratively within biostatistics team Qualifications: Masters/PhD in statistics or biostatistics Familiarity with SAS (mandatory) and R (Optional). Expertise in statistical methods and its applications in Clinical Research Good communication skills Ability to manage priorities effectively Attention to detail Excellent analytical/problem solving skills
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 We are hiring a Product Owner with 5–8 years of experience to help define, prioritize, and deliver AI-powered authoring solutions for clinical trial documentation. You will support the development of the Veridix Authoring Agent, a GenAI product that accelerates the creation of clinical documents like protocols, SAPs, CSRs, and safety reports. This role serves as a key liaison between product management, engineering, clinical experts, and AI teams to ensure delivery of compliant, usable, and high-impact authoring tools for sponsors and internal teams. The ideal candidate will have experience working on AI-driven or data-centric healthcare applications, a deep understanding of agile product practices, and a strong interest in transforming clinical trial operations with generative AI technologies. Responsibilities: Own and manage the product backlog for AI-driven clinical trial document authoring capabilities, including document drafting, review workflows, and expansion across document types. Translate product and clinical requirements into detailed epics, user stories, and testable acceptance criteria. Collaborate with engineering, AI/ML teams, QA, and clinical SMEs to deliver validated features in fast, iterative releases. Drive agile ceremonies such as backlog refinement, sprint planning, and retrospectives in coordination with scrum master and cross-functional teams. Ensure authoring solutions support compliance with regulatory standards (e.g., GCP, 21 CFR Part 11, HIPAA) and audit-readiness. Validate feature priorities with product managers, clinical users, and internal experts across domains (medical writing, biostatistics, regulatory). Help define and track product KPIs such as draft quality, turnaround time, and user adoption. Coordinate user acceptance testing (UAT), support training materials, and ensure proper documentation of releases. Contribute to long-term product strategy and roadmap for AI-enabled authoring workflows and modular document automation. Qualifications: Bachelor’s or Master’s degree in Life Sciences, Engineering, Computer Science, or a related field. 8-10 years of experience as a product owner or product manager in clinical research, digital health, or healthcare SaaS. Ability to work with UX/UI designers, backend/frontend engineers, data scientists, SQA and Product Managers. Strong understanding of agile development processes, Jira-based workflows, and product lifecycle best practices. Experience writing user stories and managing end-to-end sprint execution with cross-functional teams. Exposure to AI/ML or LLM-based technologies, especially for content generation or automation, is a strong plus. CONNECT WITH US! Follow us on Twitter - @EmmesCRO Find us on LinkedIn - Emmes #LI-Remote
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 We are hiring a Product Owner with 5–8 years of experience to help define, prioritize, and deliver AI-powered authoring solutions for clinical trial documentation. You will support the development of the Veridix Authoring Agent, a GenAI product that accelerates the creation of clinical documents like protocols, SAPs, CSRs, and safety reports. This role serves as a key liaison between product management, engineering, clinical experts, and AI teams to ensure delivery of compliant, usable, and high-impact authoring tools for sponsors and internal teams. The ideal candidate will have experience working on AI-driven or data-centric healthcare applications, a deep understanding of agile product practices, and a strong interest in transforming clinical trial operations with generative AI technologies. Responsibilities: Own and manage the product backlog for AI-driven clinical trial document authoring capabilities, including document drafting, review workflows, and expansion across document types. Translate product and clinical requirements into detailed epics, user stories, and testable acceptance criteria. Collaborate with engineering, AI/ML teams, QA, and clinical SMEs to deliver validated features in fast, iterative releases. Drive agile ceremonies such as backlog refinement, sprint planning, and retrospectives in coordination with scrum master and cross-functional teams. Ensure authoring solutions support compliance with regulatory standards (e.g., GCP, 21 CFR Part 11, HIPAA) and audit-readiness. Validate feature priorities with product managers, clinical users, and internal experts across domains (medical writing, biostatistics, regulatory). Help define and track product KPIs such as draft quality, turnaround time, and user adoption. Coordinate user acceptance testing (UAT), support training materials, and ensure proper documentation of releases. Contribute to long-term product strategy and roadmap for AI-enabled authoring workflows and modular document automation. Qualifications: Bachelor’s or Master’s degree in Life Sciences, Engineering, Computer Science, or a related field. 8-10 years of experience as a product owner or product manager in clinical research, digital health, or healthcare SaaS. Ability to work with UX/UI designers, backend/frontend engineers, data scientists, SQA and Product Managers. Strong understanding of agile development processes, Jira-based workflows, and product lifecycle best practices. Experience writing user stories and managing end-to-end sprint execution with cross-functional teams. Exposure to AI/ML or LLM-based technologies, especially for content generation or automation, is a strong plus. CONNECT WITH US! Follow us on Twitter - @EmmesCRO Find us on LinkedIn - Emmes #LI-Remote
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 Associate IT Operations Administrator will support the management of IT systems, infrastructure, and user services. This role involves providing support to users on various IT applications and projects, troubleshooting issues, assisting with onboarding, maintaining IT operations, and collaborating with senior IT staff and IT Mangar to improve technology processes. Responsibilities: Perform user onboarding and offboarding processes, including account creation, access provisioning, laptop setup, and IT orientation. Configure devices such as laptops, mobiles, and iPads for end users. Be the first point of contact for IT support via email, calls, and ticketing systems. Provide remote IT support to users to ensure timely resolution of issues. Assist users with password resets, account lockouts, Multi-Factor Authentication (MFA), and related access issues. Troubleshoot access and permissions-related issues. Troubleshoot hardware, network, and application issues, ensuring timely resolution. Troubleshoot application-related issues and escalate to Level 2 support, product team, or manager as required. Support the testing, troubleshooting, and deployment of new applications. Monitor and troubleshoot system, network, and application performance issues. Participate in patch management, software updates, and routine system maintenance tasks. Provide support for IT projects, application implementations, and technology initiatives. Assist in creating and maintaining IT incident reports. Track and manage IT incidents, ensuring timely resolution and proper documentation. Maintain IT documentation, reports, and knowledge base articles. Deliver IT training sessions and support user awareness programs. Provide regular updates to senior IT staff, product team, and manager regarding ongoing operations, issues, and projects. Follow IT policies, procedures, and compliance standards. Collaborate with cross-functional teams to support IT initiatives and continuous improvement. Assist in IT asset management, including tracking inventory, deployment, and lifecycle of hardware and software. Qualifications: B.E / B. Tech in Computer Science, Electronics & Communication, or Information Technology or equivalent. At least one year of experience in a related field Basic knowledge of operating systems (Windows, Linux, Mac) and networking fundamentals. Familiarity with cloud technologies and services. Understanding of enterprise applications, databases, and IT security concepts. Experience or willingness to learn Microsoft 365, Active Directory, AAD and Intune administration. Managing applications access and providing support via mobile devices (Android, iPhone, iPad). Strong analytical, troubleshooting, and problem-solving skills. Ability to provide IT support via multiple channels (face-to-face, email, ticketing systems and remote). Strong verbal and written communication skills. Excellent collaboration and teamwork skills. Eagerness to learn, adapt, and grow in a dynamic global environment. Willingness and ability to work in rotation shifts, including night shifts, if required. Ability to document processes, create knowledge articles, and maintain IT reports. CONNECT WITH US! Follow us on Twitter - @EmmesCRO Find us on LinkedIn - Emmes
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 IT Operations Administrator will manage and maintain the organization’s IT systems, infrastructure, and user services to ensure smooth and reliable operations. This role involves providing technical support to users, administering enterprise applications, assisting in IT projects, and collaborating with senior IT staff to implement and optimize IT processes. This position requires a strong understanding of system administration, networking, cloud services, and IT operations best practices. Responsibilities: Perform user onboarding and offboarding, including account creation, access provisioning, laptop setup, and IT orientation. Configure and maintain user devices, including laptops, desktops, mobiles, and tablets. Manage application access and provide support on mobile devices (Android, iPhone, iPad). Support procurement, inventory management, and lifecycle tracking of IT assets (hardware and software). Manage and maintain office IT infrastructure, including server rooms, conference rooms, and networking equipment. Provide IT support for hardware, software, and network issues via face-to-face, email, ticketing systems, and remote access. Track and manage IT incidents, ensuring timely resolution and proper documentation. Deliver IT training sessions and support user awareness programs. Maintain IT documentation, knowledge base articles, and reports. Administer enterprise applications, Microsoft 365, Active Directory, Intune, and other IT infrastructure components. Monitor and troubleshoot system, network, and application performance issues to ensure smooth IT operations. Support software deployment, patch management, and mobile device management (MDM). Support automation and scripting tasks (e.g., PowerShell, Bash) under guidance. Assist in IT projects, upgrades, and deployment of new systems or applications. Assist in testing, troubleshooting, and implementing new applications. Evaluate and recommend new technologies or tools to improve IT operations efficiency. Coordinate with vendors and service providers for IT equipment, software, and network services. Support vendor management, including coordinating services, SLAs, and issue resolution. Ensure IT policies, procedures, and compliance standards are followed. Assist in IT audits and ensure compliance with organizational policies and regulatory requirements. Provide regular updates to senior IT staff, product management, and the IT Manager regarding operations, incidents, and ongoing projects. Collaborate with cross-functional teams to support IT initiatives and continuous improvement. Qualifications: B.E / B. Tech in Computer Science, Electronics & Communication, or Information Technology or equivalent. 3+ years of relavant expereince. Strong knowledge of operating systems (Windows, Linux, Mac) and networking fundamentals. Experience in managing enterprise applications, cloud services, and IT infrastructure. Understanding of Active Directory, Microsoft 365, Intune, and endpoint management. Experience in managing application access and providing support on mobile devices (Android, iPhone, iPad). Knowledge of IT security principles, patch management, and compliance standards. Experience in IT asset management, software deployment, and mobile device management (MDM). Experience in monitoring, troubleshooting, and maintaining system, network, and application performance. Ability to provide IT support via multiple channels (face-to-face, email, ticketing systems, remote). Strong analytical, troubleshooting, and problem-solving skills. Ability to assist in creating and maintaining IT incident reports. Ability to document processes, create knowledge articles, and maintain IT reports. Strong verbal and written communication skills. Excellent collaboration and teamwork skills across global teams. Willingness and ability to work in rotation shifts, including night shifts, if required. Eagerness to learn, adapt, and contribute to continuous improvement of IT operations. CONNECT WITH US! Follow us on Twitter - @EmmesCRO Find us on LinkedIn - Emmes