Novotech, a globally recognized CRO (Contract Research Organization) specializing in clinical trials and drug development, is inviting applications for the position of Clinical Data Programmer I (SAS) in Bangalore, India.
This opportunity is ideal for professionals interested in clinical data management, SAS programming, and clinical trial data processing while ensuring compliance with Good Clinical Data Management Practices (GCDMP).
The Clinical Data Programmer I (CDP-I) will work within the Data Management department, supporting clinical trial projects through programming, validation, and regulatory-compliant data processes.
Job Overview
| Parameter | Details |
|---|---|
| Position | Clinical Data Programmer I (SAS) |
| Company | Novotech |
| Job Location | Bangalore, Karnataka, India |
| Employment Type | Full-time |
| Department | Clinical Data Management |
| Job ID | 3756 |
| Posted Date | 16 March 2026 |
Key Responsibilities
The Clinical Data Programmer I will support clinical trial data programming activities, including:
- Develop and maintain SAS programs for clinical data management.
- Support data cleaning, validation, and reporting activities for clinical trial datasets.
- Generate clinical data listings, reports, and data extracts for internal teams.
- Ensure compliance with Good Clinical Data Management Practices (GCDMP).
- Assist in database validation, quality checks, and discrepancy management.
- Collaborate with clinical data managers, statisticians, and project teams.
- Maintain documentation and programming standards aligned with clinical trial regulatory requirements.
- Support clinical trial database lock preparation and data integrity checks.
Required Qualifications
Candidates interested in the Clinical Data Programmer job at Novotech should have:
- Bachelor’s or Master’s degree in Life Sciences, Pharmacy, Biostatistics, Computer Science, or related field
- Knowledge of SAS programming in clinical trials
- Understanding of clinical data management processes
- Familiarity with GCDMP and clinical trial data standards
- Strong analytical and data validation skills
- Good communication and teamwork abilities
Preferred Skills
Employers may prioritize candidates with:
- Experience in clinical trial data programming
- Knowledge of CDISC standards (SDTM / ADaM)
- Experience with clinical databases or EDC systems
- Familiarity with clinical data validation and reporting
Salary and Benefits
For the Clinical Data Programmer I role in Bangalore, the estimated salary range typically includes:
- ₹6,00,000 – ₹9,00,000 per year (approx.)
- Health and wellness benefits
- Exposure to global clinical trials
- Professional training and certification support
- Opportunities for career advancement within Novotech
Why Join Novotech?
Novotech is a leading global CRO specializing in clinical development and regulatory services, known for its strong presence in Asia-Pacific clinical research markets.
Working with Novotech provides:
- Experience with global clinical trials
- Exposure to advanced clinical data management technologies
- Opportunities to collaborate with international regulatory teams
How to Apply
