17 Cdms Jobs

Premier Research is seeking an Associate Database Developer for an 8-month contract in India to join the Functional Services Provider (FSP) team. In this role, you will contribute to the transformation of life-changing ideas from biotech, medtech, and specialty pharma companies into new medicines, devices, and diagnostics. Your work will play a crucial role in saving and enhancing lives, and we value our team members as our most important asset for achieving success. We are committed to supporting your growth, providing you with the necessary skills and opportunities to thrive at work while maintaining the flexibility and balance that your life demands. Your input shapes our work culture, an...

Position: Clinical Systems Specialist Overview: We are looking for a skilled Clinical Systems Specialist with strong, hands-on experience in Veeva Testing. This role focuses on testing and validation within the Veeva environment and supports various modules in the Veeva CDMS suite. While deep experience with eCOA (electronic Clinical Outcome Assessments) and IRT (Interactive Response Technology) platforms is not required, you should understand how they work within decentralized clinical trials (DCTs) and be comfortable working alongside these systems. Job Description: Key Responsibilities: Perform testing and validation activities within Veeva CDMS , including writing and executing test scri...

At MetLife, we seek to make a meaningful impact in the lives of our customers and our communities. The Global Technology & Operations group (GTO) is a diverse team of engineers, developers, business analysts, claims analysts and project managers with the freedom to create innovative and solutions to address core business challenges with MetLife. This role will work with claimants, physicians, employers, and customers to ensure strict adherence in determining functional abilities. Provides recommendations regarding claimants current/potential functional abilities and develops goal-focused return-to-work plans. To apply, Call HR Parvez at 9810332844 Job Responsibilities Provides professional m...

You are an experienced Veeva Vault Clinical Engineer with a minimum of 5 years of experience, seeking a full-time position in Bengaluru, India with a hybrid work model of 2 days per week in the office. Your expertise lies in CTMS, eTMF, and CDMS (EDC) within the Veeva Vault ecosystem. In this role, you will be responsible for configuring, integrating, and supporting Veeva Vault Clinical applications to enhance clinical trial systems and ensure the smooth execution of clinical operations. Your key responsibilities will include configuring and supporting Veeva Vault Clinical applications such as CTMS, eTMF, and CDMS (EDC), as well as performing system integrations, connections, and enhancement...

ZS is a place where passion changes lives. As a management consulting and technology firm focused on improving life and how we live it, we transform ideas into impact by bringing together data, science, technology and human ingenuity to deliver better outcomes for all. Here you'll work side-by-side with a powerful collective of thinkers and experts shaping life-changing solutions for patients, caregivers and consumers, worldwide. ZSers drive impact by bringing a client-first mentality to each and every engagement. We partner collaboratively with our clients to develop custom solutions and technology products that create value and deliver company results across critical areas of their busines...

ZS is a place where passion changes lives. As a management consulting and technology firm focused on improving life and how we live it, our most valuable asset is our people. Here you'll work side-by-side with a powerful collective of thinkers and experts shaping life-changing solutions for patients, caregivers, and consumers, worldwide. ZSers drive impact by bringing a client-first mentality to each and every engagement. We partner collaboratively with our clients to develop custom solutions and technology products that create value and deliver company results across critical areas of their business. Bring your curiosity for learning; bold ideas; courage and passion to drive life-changing i...

Job Description for the Current running requirement of Clinical Systems Tester Veeva CDMS / Decentralized Clinical Trials (DCT). Job Title: Clinical Systems Tester Veeva CDMS / Decentralized Clinical Trials (DCT) Experience: 6+ years Location: Remote 100% Work Timing: US EST time zone Job Description: - Clinical Systems Tester Veeva CDMS / Decentralized Clinical Trials (DCT) Overview: We are looking for a well-rounded Clinical Systems Tester with core expertise in Veeva CDMS (EDC) and strong hands-on experience with eCOA and IRT platforms. This role supports testing and validation activities within a Decentralized Clinical Trial (DCT) environment, requiring flexibility across various digital...

At MetLife, we seek to make a meaningful impact in the lives of our customers and our communities. The Global Technology & Operations group (GTO) is a diverse team of engineers, developers, business analysts, claims analysts and project managers with the freedom to create innovative and solutions to address core business challenges with MetLife. This role will work with claimants, physicians, employers, and customers to ensure strict adherence in determining functional abilities. Provides recommendations regarding claimants current/potential functional abilities and develops goal-focused return-to-work plans. To apply, Call HR Nikita Grover at 8800307658 Job Responsibilities Provides profess...

Position: Clinical Systems Tester Veeva CDMS / Decentralized Clinical Trials (DCT) Overview: We are looking for a well-rounded Clinical Systems Tester with core expertise in Veeva CDMS (EDC) and strong hands-on experience with eCOA and IRT platforms. This role supports testing and validation activities within a Decentralized Clinical Trial (DCT) environment, requiring flexibility across various digital systems and patient-facing technologies. Job Description: Key Responsibilities: Author and execute test scripts in Veeva EDC, aligned with protocol requirements Validate workflows across eCOA (electronic Clinical Outcome Assessments) and IRT (Interactive Response Technology) platforms Particip...

Our team has deep understanding of EDC tools like Rave, Veeva, InForm, openClinica, clinical data repositories like SAS LSAF, Oracle LSH, eCS elluminate, Metadata Repositories like Nurocor, Sycamore, Formedix, statistical computing environments like Sycamore, Domino, Sas Viya systems, Clinical data review systems, RBQM systems, and more. With experience as solution architects, business analysts, or techno-functional SMEs in GXP compliant validated environments, they guide the creation of solution, data flows and strategies for building clinical development and data management systems. Their offerings encompass technical advisory, consultancy, developing of clinical data platforms and product...

Hi, We are hiring for the ITES Company for the Clinical SAS + SQL Programmer Profile. Job Description: Minimum 4 years of experience in any CDMS application. To perform a wide range of Clinical Data Management activities resulting in high quality database within stipulated timelines. To provide expertise in programming concepts to the Data Management team Must be able to develop the connection with the stake holders by pro-actively communicating over the calls and handling the queries by resolving them on the spot or later depending on the nature of the problem. Must be able to contribute the solutions to the DMs or Medical scientist for their New requirements either programmatically or conv...

Clinical SAS + SQL Programmer 2-8 Years of experience Mumbai/Pune/Bangalore/Hyderabad | BPO 4/5 (11-16 LPA) Req: SAS macros, SDTM/ADAM/TLFs, Oracle/PL SQL, CDMS (e.g., Inform). Required Candidate profile Must have international BPO experience. Ex-TCS ineligible. Role: Lead DM programming, automate SAS macros, ensure data quality, train teams, and adhere to SOPs. Pharma/CS/Math grad preferred.

Perform comprehensive data management tasks, Validation, Data transfers and quality control procedures. Provide Clinical Data Management team with technical expertise. Perform tasks as communicated by TL/LDM Create/review the Data Management Plans Required Candidate profile Graduate/Postgraduate in Computer Science/Computer Application/Physics/Math/Life Sciences/Pharmacy 2-8 years of experience in Statistical (SAS) programming International BPO experience is mandatory

Job Title: Veeva Vault Clinical Engineer Experience: 5+ Years Location: Bengaluru, India (Hybrid 2 days/week in office) Note: Immediate to 30-day joiners preferred. About the Role: We are looking for an experienced Veeva Vault Clinical Engineer with a strong background in CTMS, eTMF, and CDMS (EDC) . The ideal candidate will have hands-on experience in Veeva Vault configuration, integration, and support activities. Youll work closely with cross-functional teams to support and enhance clinical trial systems, contributing to the smooth execution of clinical operations. Key Responsibilities: Configure and support Veeva Vault Clinical applications including CTMS , eTMF , and CDMS (EDC) . Perform...

Hi, We are hiring for the ITES Company for the Clinical SAS + SQL Programmer Profile. Job Description: Minimum 4 years of experience in any CDMS application. To perform a wide range of Clinical Data Management activities resulting in high quality database within stipulated timelines. To provide expertise in programming concepts to the Data Management team Must be able to develop the connection with the stake holders by pro-actively communicating over the calls and handling the queries by resolving them on the spot or later depending on the nature of the problem. Must be able to contribute the solutions to the DMs or Medical scientist for their New requirements either programmatically or conv...

Hi, We are hiring for the ITES Company for the Clinical SAS + SQL Programmer Profile. Job Description: Minimum 4 years of experience in any CDMS application. To perform a wide range of Clinical Data Management activities resulting in high quality database within stipulated timelines. To provide expertise in programming concepts to the Data Management team Must be able to develop the connection with the stake holders by pro-actively communicating over the calls and handling the queries by resolving them on the spot or later depending on the nature of the problem. Must be able to contribute the solutions to the DMs or Medical scientist for their New requirements either programmatically or conv...

Hands-on Technical SME for Clinical Operations Area of expertise: Clinical early phase systems and associated study supported tools Knowledge with study set up, participant enrollment, randomization, investigational product dispensing, trial supply inventory management and participant visit tracking. Hand on experience with Evident IQ Marvin, Planisware, Almac IRT, SOCAR eSOCDAT, Clinical ink eLAS. Experience with Veeva Clinical CTMS, eTMF, and CDMS systems. Knowledge of SQL, database management, and data analysis . Familiarity with clinical data standards (e.g., CDISC, SDTM ). Experience with cloud-based solutions and SaaS platforms. Understanding of GxP, 21 CFR Part 11 , and other regulato...