Clinical Data Programmer Job at Novotech | Apply Today
Are you an experienced Clinical Data Programmer looking for an exciting opportunity in a global Contract Research Organization (CRO)? Novotech is hiring a Clinical Data Programmer II in India to support clinical trials across multiple therapeutic areas. If you have expertise in clinical data programming, EDC systems, and data management, this role offers a great opportunity to grow your career in the clinical research industry. Apply today!
About Novotech
Novotech is a global full-service clinical Contract Research Organization (CRO) dedicated to providing high-quality clinical development services. With offices in 11 geographies and site partnerships with key medical institutions, Novotech offers a wide range of services across all clinical trial phases and therapeutic areas. Novotech provides clinical development services across various phases and therapeutic areas, with a focus on IT security and quality standards. With a global presence and a team of over 3000 employees, Novotech aims to deliver excellence in clinical trials.
Novotech with extensive experience in clinical projects, phase I to IV trials and bioequivalence studies. With a strong presence in Asia-Pacific, North America, and Europe, Novotech is well-positioned to support biopharmaceutical clients worldwide. If you are passionate about clinical
research and seeking a dynamic opportunity in a global CRO, we encourage you to apply for the position of Clinical Data Programmer II.Job Description
Job Post: Clinical Data Programmer II
Location: India
The core responsibility for this position is as a member of the Data Management department at Novotech. The (Senior) Clinical Data Programmer will be responsible for programming activities on clinical trial projects and ensuring compliance with Good Clinical Data Management Practices (GCDMP).
Minimum Qualifications & Experience:
- Graduate in information science or life science-related field or similar. Two years experience in a similar role in a CRO or pharmaceutical company.
- Preferably with hands-on experience with Custom Functions/C# and Veeva EDC.
Responsibilities:
- Design and implement clinical databases
- Program data review listings and data reconciliation
- Ensure compliance with quality standards per SOPs and ICH-GCP
- Develop, validate, and maintain clinical trial databases
- Perform external data loads and liaise with vendors
Novotech is proud to offer a great workplace with a commitment to gender equality, inclusivity, and providing support for its team members. We are looking for individuals passionate about clinical research and biotech, including those from diverse backgrounds.
Keywords: Clinical Data Programmer II, Novotech, CRO, clinical trials, data management, GCDMP, C# programming, Veeva EDC, IT security, biopharmaceutical, Asia-Pacific
