Novotech Clinical Data Programmer For BSc – Apply Now!
Senior Clinical Data Programmer
Location: India
Job Description
Brief Position Description:
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:
- Designing and implementing clinical databases for projects.
- Programming of data review listings and data reconciliation.
- Ensuring quality standards are met as per SOPs and ICH-GCP guidelines.
- Designing, programming, testing, and maintaining clinical trial databases in various clinical trial applications per Novotech standards.
- Performing external data loads (e.g., labs, ECGs) as needed.
- Acting as a liaison with vendors to establish data transfer specification standards.
- Ensuring all programming activities and processes comply with standard operating procedures and good programming practices.
- Developing, validating, and maintaining clinical trials in different EDC applications.
- Annotating CRFs in line with CDISC-published or sponsor-specific guidelines, including appropriate metadata to reflect case report tabulation (CRT) data sets.
Keywords: clinical data programmer, clinical trial projects, data management, good programming practices, EDC applications, Novotech. Novotech Clinical Data Programmer For BSc – Apply Now! Please ensure you are subscribed to the Biotecnika Times Newsletter and our YouTube channel to be notified of the latest industry news. Follow us on social media like Twitter, Telegram, Facebo
