CDM Programmer II
Company: Thermo Fisher Scientific
Work Schedule: Standard (Monday–Friday)
Work Environment: Office-based
Industry: Clinical Research / CRO / Pharma Services
Expected Salary
₹5–12 LPA CTC (typically ₹6–10 LPA for candidates with 2+ years of CDM programming / SAS / SQL experience)
Role Overview
The CDM Programmer II works in Clinical Data Management (CDM) teams to design, build, and maintain clinical trial databases and edit checks using tools like Veeva EDC and programming languages such as SAS and SQL. The role supports end-to-end clinical study data deliverables and ensures high-quality, compliant clinical data processing.
Key Responsibilities
Clinical Database Development
Design, build, and test clinical trial databases.
Develop and validate edit checks using Veeva EDC.
Handle post-production changes and support full study lifecycle deliverables.
Data Programming & Processing
Define and import clinical trial data into systems.
Create and test data review listings.
Perform programming tasks aligned with study requirements.
Technical Support & Problem Solving
Work on moderately complex studies under supervision.
Troubleshoot data and programming issues.
Apply new tools and techniques to improve efficiency.
Process Improvement
Contribute to automation and process optimization initiatives.
Improve programming workflows and efficiency of CDM operations.
Participate in development of internal training materials.
Compliance & Quality
Follow GCP guidelines and SOPs.
Ensure data integrity, accuracy, and regulatory compliance.
Required Qualifications
Education
Bachelor’s degree in Life Sciences, Computer Science, Statistics, or related field.
Experience
2+ years in clinical data management, CDM programming, or related analytics roles.
Technical Skills
Programming & Tools
SAS (must have working knowledge)
SQL (relational databases)
Crystal Reports (preferred)
JReview (preferred)
Veeva EDC (highly preferred)
Core Knowledge
Clinical trial data structures
Good Clinical Practice (GCP)
Database design and validation logic
Key Skills
Strong attention to detail
Analytical and problem-solving ability
Ability to manage multiple deadlines
Strong organizational and documentation skills
Basic leadership and coordination capability
Ability to work in cross-functional teams
Preferred Qualifications
Experience in CRO or pharmaceutical clinical trials.
Exposure to global studies (multi-country trials).
Knowledge of data visualization or reporting tools.
Strong understanding of clinical research workflows.
Ideal Candidate Profile
Early-career clinical data or programming professional.
Strong SAS/SQL exposure.
Interested in clinical trials, data systems, and healthcare analytics.
Detail-oriented with strong compliance mindset.
Comfortable working in structured, regulated environments.
Career Growth
CDM Programmer → Senior CDM Programmer → Lead Programmer → Clinical Data Manager → Associate Director (Clinical Data Systems)
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