Are you a skilled 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 contribute to cutting-edge clinical trials. If you have experience in EDC systems, C# programming, and clinical data management, this could be your next career move!
Job Description
Key Responsibilities:
- Design, program, test, and maintain clinical trial databases in compliance with ICH-GCP and Novotech standards.
- Develop and validate Electronic Data Capture (EDC) systems, preferably Veeva EDC.
- Program data review listings and perform data reconciliation.
- Manage external data loads (labs, ECGs, etc.) and liaise with vendors for data transfer specifications.
- Ensure adherence to Good Clinical Data Management Practices (GCDMP) and SOPs.
- Annotate Case Report Forms (CRFs) following CDISC or sponsor-specific guidelines.
Minimum Qualifications & Experience:
- Graduate in Information Science, Life Sciences, or related field.
- 2+ years of experience in a CRO or pharmaceutical company.
- Hands-on experience with Custom Functions, C#, and Veeva EDC (preferred).
- Knowledge of CDISC standards and clinical trial data management.
Why Join Novotech?
Novotech is a leading global CRO specializing in clinical research and biotech. With 34 offices worldwide, we provide end-to-end clinical trial services across all phases and therapeutic areas.
Employee Benefits:
✅ Flexible working options
✅ Paid parental leave (for both parents)
✅ Wellness programs & career development
✅ Inclusive workplace (LGBTIQ+ friendly, disability support)
How to Apply?
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