2347 Life Sciences Jobs - Page 31

Location: Hyderabad Experience: 2-4 years Qualifications: Bachelor s/Master s in Pharmacy, Life Sciences, or related fields About the Role: Join our team to manage and oversee clinical projects, particularly in bioavailability and bioequivalence (BA/BE) studies. Key Responsibilities: Lead project management for BA/BE studies. Ensure compliance with protocols and regulatory standards. Collaborate with cross-functional teams for successful study execution. Apply Now Location: Hyderabad Experience: 2-4 years Qualifications: Bachelor s/Master s in Pharmacy, Life Sciences, or related fields

Apply Job Type Full-time Description Surgery Coder (MC) - Surgery Coding Hyderabad, Telangana Medical Coding Description nimble solutions is a leading provider of revenue cycle management solutions for ambulatory surgery centers (ASCs), surgical clinics, surgical hospitals, and anesthesia groups. Our tech-enabled solutions allow surgical organizations to streamline their revenue cycle processes, reduce administrative burden, and improve financial outcomes. Join more than 1,100 surgical organizations who trust nimble solutions and its advisors to bring deep insights and actionable intelligence to maximize their revenue cycle. In the role of Medical Coder, this individual will be responsible for the following: Perform a variety of activities involving the coding of medical records by ascribing accurate diagnosis and CPT codes as per ICD-10 and CPT-4 systems of c oding Perform Coding for records pertaining to surgeries performed with a minimum of 96% accuracy and as per turnaround time requirements Exceeds the productivity standards for Medical Coding for Surgery - as per the productivity norms for inpatient and/or specialty specific outpatient coding standards Maintains high degree of professional and ethical standards Focuses on continuous improvement by working on projects that enables customers to arrest revenue leakage while being in compliance with the standards Focuses on updating coding skills, knowledge, and accuracy by participating in coding team meetings and educational conferences Requirements To be considered for this position, applicants need to meet the following qualification criteria: Graduates in life sciences with 2 - 8 years of experience in Medical Coding for Surgery specialty Experience in Surgery coding is required Exposure to CPT-4, ICD-9 and ICD-10 Certification is not mandatory Good knowledge of medical c oding systems and regulatory requirements

About the job Our Team: Sanofi Business Operations (SBO) is an internal Sanofi resource organization setup to centralize processes and activities to support Specialty Care, Vaccines, General Medicines, CHC, CMO, and R&D, Data & Digital functions. SBO strives to be a strategic and functional partner for tactical deliveries to Medical, HEVA, and Commercial organizations in Sanofi, Globally. Main responsibilities: The overall purpose and main responsibilities are listed below: To support scientific writing team members in various deliverables to maintain clarity, coherence, correctness, and consistency while making corrections/edits in grammar, usage, punctuation, and syntax People: (1) Serve as a subject matter expert in copyediting scientific medical documents, including abstracts, posters, manuscripts, and related materials; (2) Oversee and ensure the highest level of editorial quality and adherence to industry standards and guidelines; (3) Mentor a team of junior copyeditors, providing guidance, training, and feedback on their work; (4) Maintain and plan the overall demand of copy editing requirements and vendor management for overflowing requirements for seamless execution and prioritization; (5) Develop and implement editing strategies and guidelines to enhance the overall quality and clarity of scientific content; (6) Collaborate with stakeholders to refine complex scientific concepts and ensure accuracy in content; (7) Conduct thorough fact-checking and cross-referencing of data, citations, references, and sources; (8) Stay updated with the latest advancements in scientific research, publishing trends, and evolving editing techniques; (9) Serve as a resource for resolving complex language, formatting, and scientific content-related issues; (10) Maintain effective relationships with the Writers (medical scientific community) within the allocated TA(s)/GBU(s) and product; (11) Ensure new technologies are leveraged Performance: (1) Act as strategic copyediting partner to 1 therapeutic areas (TAs) within an assigned GBU; (2) Develop and maintain expertise in 1 TA and on key trends/developments in the industry; (3) Support the development of tools, technology, and processes in order to constantly improve quality of documents from the copyediting perspective Process: (1) Contribute to overall quality enhancement by ensuring high copyediting standards and adhering to the timelines, and technical standards (Journal/congress guidelines) for the output produced by the scientific writing group; (2) Support end-to-end process through PromoMats and iEnvision, as and when required Stakeholder: (1) Maintain effective relationship with the end stakeholders (medical scientific community) with an end objective to develop quality content as per requirement About you Experience : >5 years in copyediting scientific medical documents, preferably in a professional or academic setting Soft skills : (1) Strong analytical and critical thinking skills to identify and resolve complex editing challenges; (2) Excellent attention to detail and ability to maintain consistency and accuracy across documents; (3) Strong communication and interpersonal skills to collaborate effectively with authors, researchers, and team members; (4) Ability to work independently, manage multiple projects, and meet demanding deadlines Technical skills : (1) Therapeutic area/domain knowledge exposure - Proficient in multiple therapy areas/domains under one GBU (including but not limited to): Diabetes, Dyslipidemia/ Familial hypercholesterolemia, Cardiovascular diseases, Thrombosis/atherothrombosis, Transplant, Central nervous system, Multiple sclerosis, Immunology, Oncology, Emerging markets, Generics, Vaccines, Vitamins and supplements, Digestive, Allergies, Parkinson s disease, Rare diseases, Rare blood diseases; (2) Highly proficient in the following areas: Scientific communications / writing / copyediting , Medical communications / writing / copyediting , Stakeholder management, Project management, People Management; (3) Preferred an in-depth knowledge of scientific and medical terminology, as well as industry standards and guidelines; (2) Proficiency in using relevant editing software and tools. Education : Any Bachelor s or Master s degree (preferably in Life Sciences) Languages : Exceptional command of the English language, including grammar, syntax, and punctuation At Sanofi, we provide equal opportunities to all regardless of race, colour, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, or gender identity. Watch our ALL IN video and check out our Diversity Equity and Inclusion actions at sanofi.com !

Experience: Minimum 2+ Years Location: Pune Shift: 24*7 Job Summary: The Enterprise Helpdesk Technician will be responsible for providing support and assistance to end-users within the organization. This role involves troubleshooting hardware and software issues, managing user accounts, and ensuring the smooth operation of IT systems. Primary Roles and Responsibilities: Provide first-level technical support to end-users via phone, email, and in-person. Diagnose and resolve hardware, software, and network issues. Manage user accounts, permissions, and access rights. Install, configure, and maintain computer systems and applications. Document and track support requests and resolutions using a ticketing system. Collaborate with other IT team members to resolve complex issues. Assist in the development and implementation of IT policies and procedures. Conduct training sessions for end-users on various software and hardware topics. Stay updated with the latest technology trends and advancements. Qualifications: Bachelors degree in information technology, Computer Science, or a related field Proven prior experience in a helpdesk or technical support role Strong knowledge of Windows and Mac operating systems Familiarity with network protocols, hardware, and software troubleshooting Strong knowledge and experience working with Service Now Familiarly with NICE ACD software Excellent problem-solving and communication skills Ability to work independently and as part of a team Certifications such as CompTIA A+, Network+, or Microsoft Certified Professional (MCP) are a plus. Company Profile Stratacent is a Global IT Consulting and Services firm, headquartered in Jersey City, NJ, with global delivery centres in Pune and Gurugram plus offices in USA, London, Canada and South Africa. We are a leading IT services provider focusing on Financial Services, Insurance, Healthcare and Life Sciences. We help our customers in their transformation journey and provide services around Information Security, Cloud Services, Data and AI, Automation, Application Development and IT Operations. URL - http://stratacent.com Employee Benefits: Group Medical Insurance Cab facility Meals/snacks Continuous Learning Program Stratacent India Private Limited is an equal opportunity employer and will not discriminate against any employee or applicant for employment on the basis of race, color, creed, religion, age, sex, national origin, ancestry, handicap, or any other factors. ",

Experience 3-8 years Skills - Sql and tableau, Experience with patient and claims data Location PAN India Overview You will be leading / managing a team of growing and dynamic analytics professionals whose main goal would be to help clients Marketing, Sales, and Operations leadership to achieve their business goals through data analytics. Roles and Responsibilities summary: Partner with the Clients Analytics teams to identify, scope, and execute analytics efforts that answer business questions, solve business needs, and add business value. Maintain a broad understanding of pharmaceutical sales, marketing and operations and develop analytical solutions in these areas. Manage reporting activities, build analytics-based reporting to provide enhanced business insights to clients Manage communication with stakeholders across functions and understand business requirements on regular basis Lead and guide the team independently or with little support to implement & deliver complex project assignments. Provide strategic leadership to the team by building new capabilities within the group and identifying business opportunities Set up KPI and business rules to answer business questions. Synthesize and communicate results to clients. Collaborate with client and WNS teams to implement solutions Drive analysis and problem solving and advance WNS capabilities Work with onshore and sales teams to draft proposals and solutions for clients Core competencies: Technical Skills: Advanced excel, PowerPoint, SQL, Tableau / PowerBI, Hands on experience in R / Python / SAS would be an advantage Domain knowledge in healthcare with working knowledge of various datasets used in the pharmaceutical industry Life sciences domain knowledge (2+ years) Good client communications (verbal and written) Data Analysis, Descriptive Analysis and Ability to handle Large volumes of Data for Ad-hoc analysis and Standard Business Reporting - 2+ years Knowledge of different pharma data sources - IQVIA, Flatiron, SHS, EMR / HER data, etc. Commercial Analytics Experience in Lifescience required Data analysis and Reporting capability Experience of working with offshore / onshore teams Empathy, adaptability and emotional intelligence Close attention to detail, with a quality-focused mindset Self-discipline for planning and organizing tasks Aptitude for, and enjoyment of working in teams Must have Skills: Tableau / Power BI, SQL, Excellent Communication, Excel, PowerPoint, Analytical Skills, Problem solving, Written and Verbal Communication, Stakeholder management, Work as a team Good to have Skills: Stakeholder Management, knowledge on therapy areas is an added advantage Qualifications Highest Education: Bachelors or masters degree in engineering (any branch), and strong academic performance with analytic and quantitative coursework is required

We are seeking highly motivated individuals to join our medical coding team. The ideal candidate will be responsible for reviewing and accurately coding diagnoses using ICD-10-CM for risk adjustment purposes in compliance with CMS guidelines. Industry: Medical Coding and Billing Services Healthcare Location: 3rd Floor, Indian Express Building, Banerji Rd, Kaloor, Ernakulam, Kerala 682017 Work Hours: Day Shift: 9am 6pm / Night Shift: 9pm 6am Employment Type: Full Time Salary: Best in the Industry Responsibilities: Review and analyze patient medical records to assign accurate ICD-10-CM codes for for this position Allowed Type(s): .pdf, .doc, .docx By using this form you agree with the storage and handling of your data by this website. *

159 Solutions - Consulting - Analytics Associate (0-2 yrs) About Company: 159 Solutions (an IQVIA company) is a Healthcare consulting firm that delivers a wide range of analytical solutions to Life Sciences clients to help them drive customer value and company results. We leverage our deep industry expertise coupled with thoughtful data analysis to provide customized solutions that work in the real world. We believe in delighting our customers and greatly value our people, their perspectives and new ideas. 159 Solutions has 150+ talented and motivated people working in Pune, India collaborating with our colleagues in San Mateo, CA serving life sciences companies in US. Analytics Associate Analytics Associates are active participants in analyzing the data and creating solutions for our clients to solve business problems across various practice areas such as promotion response modeling, patient claims analytics, sales force strategy, incentive compensation, business intelligence, modeling Key Responsibilities Process large-scale healthcare datasets using Alteryx, SQL, other database management tools Analyze the data and design custom solutions to uncover insights and solve client s problem Develop recommendations for the client and create PowerPoint slides or online visualization (e.g. Tableau, Qlikview, Sisense etc.) to communicate results to clients and internal teams Collaborate with internal teams and others to learn new skills and train others Qualifications Bachelors degree in any engineering discipline [OR] MSc/BSc/B.Pharma from top tier (IIT/NIT) schools [OR] 0-1 years of work experience in analytics Individuals should also have The Following Personal Skills: High motivation, strong work ethic and positive attitude Quick learner with dedication to continuous learning Strong problem-solving skills Client service orientation with focus on quality and detail Excellent task management skills Good communication skills with fluency in English Ability to work across global cross-office teams IQVIA offers a competitive compensation package with salary and bonus incentives, plus an attractive benefits package.

Project Analyst II, Bangalore/Chennai ICON plc is a world-leading healthcare intelligence and clinical research organization. We re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organisations. With our patients at the center of all that we do, we help to accelerate the development of drugs and devices that save lives and improve quality of life. With our patients at the center of all that we do, we help to accelerate the development of drugs and devices that save lives and improve quality of life. Our people are our greatest strength, are at the core of our culture, and the driving force behind our success. ICON people have a mission to succeed and a passion that ensures what we do, we do well. The Role: The Project Analyst II at ICON supports the assigned department or functional team through the independent management of assigned projects and tasks. The Project Analyst II has a demonstrated ability to complete assigned projects and tasks and works closely with other members of the project team, client, clinical/scientific teams, and internal and external clients and vendors for successful project execution. We pride ourselves on our amazing company culture, where we work as one team to achieve industry-leading results. To be successful in the role, you will have: Bachelors Degree preferably in life sciences 2-3 years of relevant experience and/or study in Project Management or Regulatory or a related field. General Business and/or Finance-related experience is a plus. Ideally you will have experience within a clinical environment Strong IT skills, specifically with Microsoft Excel Excellent written and verbal communication skills Ability to work to tight deadline Benefits of Working in ICON: Our success depends on the knowledge, capabilities and quality of our people. Thats why we are committed to developing our employees in a continuous learning culture - one where we challenge you with engaging work and where every experience adds to your professional development. At ICON, our focus is to provide you with a comprehensive and competitive total reward package that comprises, not only an excellent level of base pay, but also a wide range of variable pay and recognition programs. In addition, our best in class employee benefits, supportive policies and wellbeing initiatives are tailored to support you and your family at all stages of your career - both now, and into the future. ICON, including subsidiaries, is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know through the form below. What ICON can offer you: Our success depends on the quality of our people. That s why we ve made it a priority to build a diverse culture that rewards high performance and nurtures talent. In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family. Our benefits examples include: Various annual leave entitlements A range of health insurance offerings to suit you and your family s needs. Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead. Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family s well-being. Life assurance Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others. Visit our careers site to read more about the benefits ICON offers. At ICON, inclusion & belonging are fundamental to our culture and values. We re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here . Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless - there s every chance you re exactly what we re looking for here at ICON whether it is for this or other roles. Are you a current ICON Employee? Please click here to apply

About the Role As a Project Support Coordinator, you will get an opportunity to wear a hat of a Project Manager & a Data Analyst. In this hybrid role, you will be coordinating with the CFTs for overseeing and managing projects from initiation to completion, ensuring they meet business goals and deadlines, while also leveraging data to drive decisions and improve processes. Skills & Core Competencies: Organized: Set priorities, develop a work schedule, monitor progress towards goals, and track details / data / information / activities. Communicate Effectively: Speak, listen, and write in a clear, thorough, and timely manner using appropriate and effective communication tools and techniques. Collaborate with CFT (Foster Teamwork): Work cooperatively and effectively with others to set goals, resolve problems, and make decisions that enhance organizational effectiveness. Make Decisions: Assess situations to determine the importance, urgency, and risks, and make clear decisions which are timely and in the best interests of the organization. Risk & Issue Management: Identify potential project risks and develop mitigation strategies. Address any issues that arise during the project lifecycle, ensuring minimal disruption to timelines and deliverables. Project Reporting & Documentation: Provide regular status updates and project reports to senior management and stakeholders. Ensure that all project documentation is organized and up to date. Data Collection & Analysis: Gather, clean, and analyze large datasets to identify trends, patterns, and insights. Transform raw data into actionable reports and dashboards. Candidate Requirements: 2-4 years of work experience Proficient in Microsoft Excel and Power Point University Degree in a related field (i.e., Business, Data, etc.) Strong problem-solving skills and the ability to think analytically and strategically. Excellent communication and interpersonal skills to effectively collaborate with cross-functional teams and stakeholders. Detail-oriented with excellent organizational and time management skills. Ability to prioritize and manage multiple tasks simultaneously while meeting deadlines.

Individual contributor with advanced knowledge acquired from several years of experience in the professional discipline. Works independently under limited supervision. Essential Functions Acts as a Regulatory Team Leader on complex projects, which may include technical writing and/or may act as a Project Manager for a stand-alone project, with guidance from senior staff as appropriate; Competently writes regulatory and/or technical documents with minimal review by senior staff; Establishes relationships with many customers; may meet face to face without rest of team to discuss regulatory issues and present lessons learned. Adopts a proactive and flexible approach to resolve any issues; Undertakes detailed review and management of budgets related to projects, including out of scope activities. Ensures revenue is recognised and challenges when appropriate, may seek guidance from senior staff as appropriate; May give guidance to junior colleagues, including feedback on the quality of technical documents, and may assist in their training and development; May present to clients at bid defense meetings by phone or in person, for a range of regulatory deliverables, at discretion of senior staff; May write new regulatory standard operating procedures, and/or propose revisions and/or act as reviewer for regulatory standard operating procedures, as assigned and appropriate. May be involved in a Regulatory and/or IQVIA Initiative; Performs other tasks or assignments, as delegated by Regulatory management; May manage meetings with Regulatory Agencies; May be assigned as Reviewer and/or Approver for Regulatory standard operating porcedures or cross-functional standard operating porcedures owned by other operations; May support global regulatory or technical initiatives or act as a regional representative on a cross-functional initiative; Performs other duties, as business needs require; Qualifications Bachelors Degree Degree in Lifescience or related discipline Req Or Masters Degree Degree in Lifescience or related discipline At least 8 years relevant experience Good understanding of the Research and Development process (Chemistry, Manufacturing & Controls, Preclinical and Clinical), laws and related guidelines, as appropriate; Possesses a specific regulatory or technical expertise. Sufficient knowledge of managing regulatory projects, project deliverables on a time bound manner; Expert in planning and delivering work on time keeping quality parameter in mind; Knowledge of regulatory procedures in appropriate region particularly marketing authorization transfers and relevant cross-functional dependencies; Good working knowledge of regional regulatory intelligence; Ability to work closely with client regional heads to determine the MAT, Regulatory Publishing & submission strategy and execute marketing authorization transfer plan, if applicable; Good understanding of pharmacovigilance activities relevant to transfer of marketing authorization; Ability to establish and maintain effective working relationships with coworkers, managers and clients; Strong software and computer skills, including Microsoft Office, publishing applications and tools, as applicable; Ability to work on several projects, with direction from senior staff as appropriate; Ability to follow standard operating porcedures consistently; provides independent thought to assist in process improvements; Ability to make decisions on discrete tasks under senior supervision; Requires advanced knowledge within a specific discipline typically gained through extensive work experience and/or education; Experience of involvement in regulatory strategy and determination of documentation requirements, timelines, budgets for MATs, Publishing projects; Project leadership experience; Makes adjustments or recommended enhancements in systems and processes to solve problems or improve effectiveness of job area; Problems faced are general and may require understanding of broader set of issues, but typically are not complex; Ability to adapt quickly to a rapidly changing environment; Applicable certifications and licenses as required by country, state, and/or other regulatory bodies

Ensure all aspects of department shipments to and from sites locally and internationally comply with applicable regulations, courier specifications and study parameters. Resolve shipping problems related to customs, FDA, dangerous goods or couriers. Ensure on-line shipping program is maintained within laboratory policy and procedural guidelines and users are trained. Assist with strategic initiatives at a local level. Essential Functions Assist with executing identified global initiatives at a local level within timelines Liaise with internal / external clients in relation to shipping regulations and logistics initiatives Advise Project Management on correct shipping materials and documentation to order for global studies Coordinate any special arrangements with couriers Gather data from PM about kit contents, site lists, etc , during protocol design and calculate shipping quantities over the life of the study Prepare commercial invoices, letters of instruction, letters to airport police, and supply pre-printed air bills to sites to ensure specimens will be shipped in compliance with each country s regulations and each courier s specifications Operate all courier systems to prepare package address labels, invoices and other associated documentation correctly in a timely manner Liaise with courier IT departments to ensure prompt rectification of any system faults Ensure system upgrades are implemented with minimum impact to business Maintain all shipping machines address databanks and keep them up-to-date Liaise closely with Project Management to ensure accurate address details in QLIMS QC all shipping documentation prior to shipping and check shipments against manifest Track and trace shipments and follow up problem shipments to ensure they are progressed and delivered rapidly Monitor inventory level requirements and maintain a minimum operating stock level for all couriers material as required Train new staff in the operation of all courier systems Monitor processes within Logistics with a view to increase quality and efficiency of current method of operation Produce all courier manifest reports each evening and ensure these are retained as a record Responsible for all record keeping and archiving of quality data Maintain filing and archiving system for all shipping material for all couriers used Maintain a record of returned/damaged shipments and ensure that appropriate claims are submitted Produce monthly metrics reports relating to the Logistics group Maintain current knowledge of customs and shipping regulations/restrictions for import/export worldwide and communicate changes effectively Maintain current knowledge regarding Dangerous Goods shipping Ensure paperwork generated by photocopying is done in a quality manner to provide a professional appearance and faxed documentation is of a professional appearance prior to faxing Qualifications High School Diploma or equivalent 2 year of related experience. Good communication and problem-solving skills. Detail-oriented, thorough, and well-organized. Ability to grasp general concepts of import/export regulations. Ability to work in a fast-paced, high-stress environment. Ability to establish and maintain effective working relationships with co-workers, managers and clients.

Brief team/department description: Technical Operations is responsible for management and oversight of technical process strategy, CMO and CDMO management, and execution of product deliverables in alignment with Azurity policies, Azurity clients and in accordance with company objectives. The position leads staff and / or contractors and collaborates cross-functionally to achieve project milestones in support of process scale-ups and process validation, technical transfers, implementation of lifecycle post approval changes, and investigation / closure of deviations / OOS for commercial products. Principle Responsibilities: Manage the planning and execution of manufacturing along with associated qualification and validation activities as they relate to both development and commercial products. In cooperation with contract facilities, manage the review, approval, and execution of controlled documentation concerning late-stage development, qualification, validation, and commercial manufacturing activities as needed. Direct tasks associated with late stage product / process development (as applicable), product transfers, equipment qualifications, and validation activities to ensure alignment with company policies and objectives. Support and / or lead product launch and commercialization efforts. Ensure that appropriate policies, SOPs and documentation are in place to support validation practices according to regulatory requirements and applicable industry guidance documents. Support Management Review and Compliance related activities as needed. Assist in preparing metrics and compiling summaries to effectively communicate status and recommendations to Senior Management. Support Due Diligence activities to support company objectives including product development, technical transfer, commercial manufacturing, and/or commercial launch. Collaborate closely with cross-functional team members from functions including Supply Chain, Product Development, Quality Assurance, and Regulatory Affairs. Qualifications and Education Requirements Bachelor s degree in Life Sciences (Master s Degree preferred), or related field. Minimum 15 years of experience in biopharmaceutical / pharmaceutical GMP environment or related industry. Expertise in cGMPs, ICH and Validation related requirements and guidances In-depth experience in performing technical transfer of multiple dosage forms (solid oral, liquid oral, injectables, etc.) Experienced in multiple validation disciplines including manufacturing process validation of multiple dosage forms, cleaning validation, packaging validation, analytical methods validation, terminal sterilization validation, hold time studies, shipping studies, equipment / utilities qualification, and facilities validation Ability to work in a strategic, tactical, and hands-on level. Candidate must be proficient in Microsoft Word, Excel, and Powerpoint. Experienced in participating in regulatory agency inspections. By applying for this role, you confirm that you are mentally and physically capable of fulfilling the job responsibilities detailed in the job description without any restrictions. If you have any concerns or even the slightest disability that may affect your ability to perform the job, please inform HR in advance.

Job Description: Service Delivery Manager - QMS Position Overview: We are seeking an experienced and strategic Service Delivery Manager to lead our global team in delivering high-quality QMS Application Management Services (AMS) support to pharmaceutical and medical device clients. This role will oversee operational delivery and client satisfaction across a suite of SaaS based Commercial and R&D technology platforms, including MDM, CRM, Data Warehousing, and Veeva Vault solutions. Core Responsibilities: Lead global managed services operations across the U.S., India, and EU, ensuring consistent, high-quality support for QMS AMS. Oversee service delivery for solutions involving QMS AMS, Veeva Vault, Salesforce, Reltio, Egnyte, Power BI, Snowflake, and SQL Server. Develop and implement service-level agreements (SLAs), KPIs, and operational excellence frameworks. Act as an executive point of contact for key clients, ensuring alignment with commercial and R&D business objectives. Provide resolutions to data issues and manage data loads into multiple client systems. Work on enhancements to existing QMS AMS. Generate technical reports as requested by the business team. Partner with internal practice leads to continuously improve service delivery models and solution offerings. Ensure compliance with relevant regulatory standards (e.g., GxP, HIPAA, 21 CFR Part 11) in service operations. Skills & Experience: 10+ years of experience in IT service delivery or managed services. Strong domain knowledge in life sciences commercial and R&D systems. Proven experience with managed services for Veeva Vault, MDM, CRM, Snowflake, DataBricks, with a deep understanding of at least three core platforms. Demonstrated ability to sit at the intersection of technology and business while driving results. Success in managing globally distributed teams and supporting enterprise clients. Excellent client-facing communication, stakeholder management, and problem-solving skills. Familiarity with regulatory requirements specific to pharmaceutical and medical device industries.

Project Analyst II, Bangalore/Chennai ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organisations. With our patients at the center of all that we do, we help to accelerate the development of drugs and devices that save lives and improve quality of life. With our patients at the center of all that we do, we help to accelerate the development of drugs and devices that save lives and improve quality of life. Our people are our greatest strength, are at the core of our culture, and the driving force behind our success. ICON people have a mission to succeed and a passion that ensures what we do, we do well. The Role: The Project Analyst II at ICON supports the assigned department or functional team through the independent management of assigned projects and tasks. The Project Analyst II has a demonstrated ability to complete assigned projects and tasks and works closely with other members of the project team, client, clinical/scientific teams, and internal and external clients and vendors for successful project execution. We pride ourselves on our amazing company culture, where we work as one team to achieve industry-leading results. To be successful in the role, you will have: Bachelors Degree preferably in life sciences 2-3 years of relevant experience and/or study in Project Management or Regulatory or a related field. General Business and/or Finance-related experience is a plus. Ideally you will have experience within a clinical environment Strong IT skills, specifically with Microsoft Excel Excellent written and verbal communication skills Ability to work to tight deadline Benefits of Working in ICON: Our success depends on the knowledge, capabilities and quality of our people. Thats why we are committed to developing our employees in a continuous learning culture - one where we challenge you with engaging work and where every experience adds to your professional development. At ICON, our focus is to provide you with a comprehensive and competitive total reward package that comprises, not only an excellent level of base pay, but also a wide range of variable pay and recognition programs. In addition, our best in class employee benefits, supportive policies and wellbeing initiatives are tailored to support you and your family at all stages of your career - both now, and into the future. ICON, including subsidiaries, is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know through the form below. Visit our careers site to read more about the benefits ICON offers. At ICON, inclusion & belonging are fundamental to our culture and values. We re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here . Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless - there s every chance you re exactly what we re looking for here at ICON whether it is for this or other roles. Are you a current ICON Employee? Please click here to apply

Clinical Data Science Lead _ Office Based We are currently seeking a Clinical Data Science Lead to join our diverse and dynamic team. As a Clinical Data Science Lead at ICON, you will play a crucial role in driving data science initiatives within clinical trials, ensuring that our analyses provide meaningful insights that inform strategic decisions. You will contribute to the advancement of innovative therapies by overseeing data science projects and leading a team of data professionals. What You Will Be Doing: Leading the design and implementation of data science strategies to enhance clinical trial data analysis. Collaborating with cross-functional teams to identify key data requirements and analytical needs. Overseeing the development of statistical models and analytical tools to optimize data interpretation. Mentoring and guiding team members in best practices for data analysis and visualization. Communicating findings and insights to stakeholders through presentations and reports, influencing project direction. Your Profile: Advanced degree in statistics, data science, life sciences, or a related field. Extensive experience in data analysis and project leadership within a clinical research setting. Strong expertise in statistical software and data visualization techniques. Exceptional analytical and problem-solving skills, with a focus on translating data into actionable insights. Excellent communication and leadership skills, with the ability to foster collaboration across diverse teams. Visit our careers site to read more about the benefits ICON offers. At ICON, inclusion & belonging are fundamental to our culture and values. We re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here . Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless - there s every chance you re exactly what we re looking for here at ICON whether it is for this or other roles. Are you a current ICON Employee? Please click here to apply

in NIRF 2024 and is placed in the band of 501 - 550 in the QS Rankings for Asia region 2024. It has received Diamond rating in the QS I Gauge India Ratings and has been ranked in the 601+ band in the Times Higher Education World University Rankings, Asia. Job Description: Candidate will be responsible for teaching undergraduate and/ or postgraduate Bioinformatics courses, guiding student research and conducting original research in the field of bioinformatics & computational biology. He/ she shall contribute to curriculum development, interdisciplinary collaborations and securing research funding. Money As per Norms Qualification M.Sc (Bioinformatics/ Biotechnology/ Life Sciences), Ph.D (preferred) Experience Minimum of three years of research/ teaching experience.

Duration Initially for a period of one year and extendable for one more year or till termination of the project whichever is earlier based on performance evaluation on yearly basis. Money 31000 + 18% HRA per month for candidates with NET or GATE or undergone selection process through National level examination conducted by Central Government Department and their agencies. For other candidates it s 25000 + HRA who do not have NET or GATE as per DST guidelines. Qualification First Class Post-Graduate Degree in Life Sciences (Microbiology/ Biotechnology/ Biochemistry etc). Experience Desirable: Candidates with prior experience in molecular biology techniques including gene cloning and protein purification will be preferred.

Clinical Data Science Lead _ Office Based ICON plc is a world-leading healthcare intelligence and clinical research organization. We re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development We are currently seeking a Clinical Data Science Lead to join our diverse and dynamic team. As a Clinical Data Science Lead at ICON, you will play a crucial role in driving data science initiatives within clinical trials, ensuring that our analyses provide meaningful insights that inform strategic decisions. You will contribute to the advancement of innovative therapies by overseeing data science projects and leading a team of data professionals. What You Will Be Doing: Leading the design and implementation of data science strategies to enhance clinical trial data analysis. Collaborating with cross-functional teams to identify key data requirements and analytical needs. Overseeing the development of statistical models and analytical tools to optimize data interpretation. Mentoring and guiding team members in best practices for data analysis and visualization. Communicating findings and insights to stakeholders through presentations and reports, influencing project direction. Your Profile: Advanced degree in statistics, data science, life sciences, or a related field. Extensive experience in data analysis and project leadership within a clinical research setting. Strong expertise in statistical software and data visualization techniques. Exceptional analytical and problem-solving skills, with a focus on translating data into actionable insights. Excellent communication and leadership skills, with the ability to foster collaboration across diverse teams. What ICON can offer you: Our success depends on the quality of our people. That s why we ve made it a priority to build a diverse culture that rewards high performance and nurtures talent. In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family. Our benefits examples include: Various annual leave entitlements A range of health insurance offerings to suit you and your family s needs. Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead. Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family s well-being. Life assurance Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others. Visit our careers site to read more about the benefits ICON offers. At ICON, inclusion & belonging are fundamental to our culture and values. We re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here . Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless - there s every chance you re exactly what we re looking for here at ICON whether it is for this or other roles. Are you a current ICON Employee? Please click here to apply

1. Conducts comprehensive patent analysis, prepare patent landscape reports and understands the scope of patent protection 2. Analysis of patent documents utilizing a knowledge of chemistry/biotechnology and chemical nomenclature coupled with knowledge of international pharmaceutical patent law 3. Monitors and analyzes patent legal status (patent expiry, withdrawals, lapses and rejections) 4. Monitors and analyzes other sources of intellectual property and regulatory monopoly, including patent extensions, marketing and data exclusivity and patent legal status (patent expiry, reassignments, withdrawals, lapses and rejections) 5. Ongoing monitoring of patent publications in accordance with standards, company priorities and the production cycle 6. Creation of Excel/VBA/Access/SQL based automation tools to increase overall process efficiency 7. Efficiently manage multiple tasks on an ongoing basis which would typically include web crawling, process improvements, quality check, advanced data analytics etc.

Who we areCitiusTech - Shaping Healthcare Possibilities.CitiusTech is a global IT services, consulting, and business solutions enterprise 100% focused on the healthcare and life sciences industry. We enable 140+ enterprises to build a human-first ecosystem that is efficient, effective, and equitable with deep domain expertise and next-gen technology. With over 8,500 healthcare technology professionals worldwide, CitiusTech powers healthcare digital innovation, business transformation, and industry-wide convergence through next-generation technologies, solutions, and products.Our PurposeWe are shaping healthcare possibilities to make our clients businesses successful, which is not just a statement but our purpose, driving us to explore what s next in healthcare.Our goal is clear: to make healthcare better for all - more efficient, effective, and equitable. We are investing in people, technology, innovation, and partnerships to create meaningful change. We see technology not just as a tool but as a catalyst that amplifies human ingenuity to solve complex healthcare challenges.100% healthcare focus | Trusted by 140+ healthcare and life sciences enterprises |40% of Fortune 500 healthcare enterprises are our clients | #1 Rated as a leader by top analyst firmsOur visionTo inspire new possibilities for the health ecosystem with technology and human ingenuity.What is in it for you?As a Senior Software Engineer - MLops, you will be a part of an Agile team to build healthcare applications and implement new features while adhering to the best coding development standards.Responsibilities: - * Monitoring Build & Production systems using automated monitoring and alarm tools * Creating and using benchmarks, metrics, and monitoring to measure and improve services. * Providing best practices and executing POC for automated and efficient model operations at scale. * Designing and developing scalable MLOps frameworks to support models based on client requirements.Experience: - * 3 - 5 YearsLocation: - * PuneEducational Qualifications: - * Engineering Degree - BE / ME / BTech / M Tech / B.Sc. / M.Sc. * Technical certification in multiple technologies is desirable.Skills: -Mandatory Technical skills * Good hands-on experience & in-depth knowledge ML flow, MLOPs * Experience on AWS sagemaker - Expected to manage database and installations * Good exposure to AWS cloud deployments * Real-World Hands-On Experience in MLOps and Data science field * Requirement understanding and effectively manage client communication Good to have skills: - * Good experience in GIT, Agile (Scrum or Kanban) * Flexible to work in evening timings * Good to have (added advantage): AWS (Multi-Region Deployments, Cloudformation) * AzureDevOps (TFS) - JIRA * Good presentation skills & communications skills * Written & verbal skills especially to confidently express technical ideas / solutions

We are looking for an experienced Medical Representative to join our team at Sunrise Remedies. The successful candidate will be responsible for promoting and selling our products to healthcare professionals and institutions. Experience: Minimum 6 Month of Gynecology And Dermatologist Segment. Industries: Pharmaceutical. Qualification: Bachelor s degree in Nursing, Pharmacy, Life Sciences, or a related field. Segment: Gynec / Derma. Headquarter Location: Ahmedabad | Vadodara |Surat | Rajkot | Mehsana | Bhavnagar | Vapi | Valsad Roles and Responsibilities Develop and maintain relationships with healthcare professionals and institutions. Promote and sell products to healthcare professionals and institutions. Develop and execute sales strategies to increase sales. Monitor market trends and competitor activities. Prepare and present sales reports. Attend conferences and trade shows. Participate in promotional events, CMEs, and training sessions. Knowledge of the medical industry.

Area Sales Manager (ASM) Gynec / Derma Gujarat We are looking for an experienced Area Sales Manager (ASM) to join our team at Sunrise Remedies. The successful candidate will be responsible for promoting and selling our products to healthcare professionals and institutions. Experience: Minimum 3 Year of Gynecology And Dermatologist Segment. Industries: Pharmaceutical. Qualification: Bachelor s degree in Nursing, Pharmacy, Life Sciences, or a related field. Segment: Gynec / Derma. Headquarter Location: Ahmedabad | Vadodara | Surat | Rajkot. Roles and Responsibilities Develop and implement effective sales strategies to achieve sales targets an d market growth. Build and manage a high-performing sales team, providing guidance and mentoring. Identify new business opportunities and develop strong relationships with key clients. Monitor market trends and competitor activities to stay ahead in the market. Collaborate with cross-functional teams to ensure the successful launch of new products. Provide timely reports and analysis to the senior management team. Develop and maintain strong relationships with distributors and stakeholders. Ensure stability and efficiency in the sales processes.

As a Technical Lead - JBoss, you will be a part of an Agile team to build healthcare applications and implement new features while adhering to the best coding development standards Responsibilities: - * Gather complete understanding of the requirements and develop a thorough understanding of the Epics/user stories intended for a Release/Sprint * Understand the current and proposed design, and prepare LLD for Epics considering the dependencies across domains * Follow best coding practices, and adhere to the code coverage metrics * Demonstrate developed piece of code * Troubleshoot production tickets that may be raised during offshore hours * Create a work breakdown structure (WBS) for epics planned in a release or sprint * Develop and analyze the code and assess work deliverables * Guide, coach Scrum teams on newer tech stacks * Collaborate with different teams Experience: - * 5 - 7 Years Educational Qualifications: - * Engineering Degree - BE/ME/ BTech/ MTech/ BSc/MSc * Technical certification in multiple technologies is desirable Skills: -Mandatory Technical skills * Java * JBoss Fuse * Apache Camel

As a Manager- Marketing, your Job responsibilities will include: * Develop and execute comprehensive partner marketing strategies that align with CitiusTechs business objectives and those of CitiusTech s technology partners * Translate market business objectives into relevant marketing campaigns, activities, and initiatives to achieve demand generation and sales enablement outcomes * Plan, design, and execute joint marketing campaigns and programs with partners, including webinars, events, content marketing, digital campaigns, and more * Own and drive a multi-channel marketing strategy for demand generation, brand visibility, and deal pursuit success * Track and support new business, deal pursuits, and enhance win rates by partnering with partnership and sales teams * Organize and manage co-branded events, including roundtables, webinars, and industry meet-ups * Ensure seamless execution of Partner engagement from maximum target audiences * Collaborate with content creators and Subject Matter Experts to develop compelling marketing materials, including thought leadership, collateral, presentations, and webinars * Identify opportunities to create vertical-specific marketing content assets, either in-house or with partners * Build and maintain strong relationships with key contacts at partner organizations * Act as the primary point of contact for all marketing-related activities with partners * Establish KPIs for partner marketing initiatives, and track performance against these metrics * Provide regular reports on the effectiveness of partner marketing activities and suggest improvements * Conduct market research to stay informed about industry trends, competitor activities, and customer needs * Use insights to refine partner marketing strategies and tactics * Own the partner marketing budget, manage funding from partners, and ensure adherence to organizational processes * Plan and provision requirements timely and efficiently * Work with sales, partnership team, and other members of the marketing team to define and implement marketing plans for the market segment * Partner with extended teams to customize and curate organizational content assets for vertical marketing purposes Experience: - * 7 - 10 Years Location: - * Bangalore * Mumbai Educational Qualifications: - * Any Bachelor s degree Skills: -Mandatory Technical Skills * This role requires a blend of strategic thinking, creativity, and hands-on execution to drive co-marketing initiatives and achieve mutual business goals * 5 + yrs of full time B2B Tech marketing experience, with hands-on experience in working with tech partners like AWS, Microsoft, GCP, and more * Proven competency in demand generation and brand awareness marketing * Practical knowledge of and experience in contemporary digital marketing channels, marketing automation tools, data analytics and reporting * Excellent communication and presentation skills with proven content curation capabilities * Ability to build collaborative partnerships and work in a matrixed and high demand environment * Self-motivated, hands on and results oriented, with a focus on outcomes and time bound delivery * Experience in managing outreach budgets

As a Solution Architect - HL7, you will be part of an agile team to build healthcare applications and implement new features while adhering to the best coding development standards Responsibilities: Architect, design, and build solutions within the healthcare domain, and specifically focus on Healthcare Information Exchange (HIE), data integration, and interoperability standards such as HL7/FHIR Lead the team of experts, drive growth, and create innovative solutions for the clients based on industry trends and evolving business needs Demonstrate a growth mindset, practice building experience, and envision and propose next-generation solutions Lead and mentor a team of experts in Healthcare Interoperability Drive practice growth by developing new offerings and proposing innovative solutions to clients Architect and design robust solutions, adhere to interoperability standards like HL7/FHIR Manage large-scale implementation projects, and ensure timely and successful delivery Projects Build and maintain strong client relationships, and act as a trusted advisor Experience: 8 - 10 Years Educational Qualifications: Engineering Degree - BE / ME / BTech / MTech / BSc / MSc Technical certification in multiple technologies is desirable Relevant certifications in HL7/FHIR are highly desirable Skills:Mandatory Technical skills Strong experience of HL7/FHIR and experience in interoperability interface engines 10+ years of extensive professional experience in Healthcare Interoperability Extensive experience in integrating healthcare systems using interface engines such as Mirth, Rhapsody, Cloverleaf, and more Proven track record of practice building, business development, and client relationship management Excellent leadership, communication, and problem-solving skills Strong business acumen and experience in practice building, business development, and client relationship management