Clinical Data Programmer I (SAS)

Why This Role Matters
Clinical Data Programmers play a key role in ensuring the accuracy, integrity, and compliance of clinical trial data. Their work directly supports drug development, regulatory submissions, and patient safety by maintaining high-quality clinical datasets. This role is especially important in bridging clinical research and data analytics within global trials.

Job Description
Novotech is hiring a Clinical Data Programmer I (SAS) in Bangalore, India. The role involves supporting clinical trial data programming, validation, and reporting while ensuring compliance with Good Clinical Data Management Practices (GCDMP). This is an excellent opportunity for professionals interested in clinical data management and SAS programming within a global CRO environment.

Key Features of the Role: Responsibilities
• Develop and maintain SAS programs for clinical data management.
• Perform data cleaning, validation, and discrepancy management.
• Generate clinical data listings, reports, and extracts.
• Ensure compliance with GCDMP and regulatory standards.
• Assist in database validation and quality checks.
• Collaborate with clinical data managers, statisticians, and project teams.
• Maintain programming documentation and standards.
• Support database lock activities and data integrity checks.

Eligibility Criteria

Educational Qualification
• Bachelor’s or Master’s degree in Life Sciences, Pharmacy, Biostatistics, Computer Science, or related field.

Experience
• Freshers or candidates with relevant experience can apply.

Required Skills
• Knowledge of SAS programming in clinical trials.
• Understanding of clinical data management processes.
• Familiarity with GCDMP and clinical trial standards.
• Strong analytical and data validation skills.
• Good communication and teamwork abilities.

Preferred Skills
• Knowledge of CDISC standards (SDTM / ADaM).
• Experience with clinical databases or EDC systems.
• Exposure to clinical trial data programming and reporting.

Salary Insights
• ₹6,00,000 – ₹9,00,000 per annum (approx.)

Benefits & Perks
• Exposure to global clinical trials.
• Health and wellness benefits.
• Professional training and certification support.
• Career growth opportunities within a global CRO.

Company Overview
Novotech is a leading global Contract Research Organization (CRO) specializing in clinical development and regulatory services. With a strong presence in the Asia-Pacific region, Novotech supports pharmaceutical and biotech companies in conducting efficient and compliant clinical trials worldwide.

FAQs

• Is SAS knowledge mandatory?
Yes, basic knowledge of SAS programming is required.

• Is this role suitable for freshers?
Yes, candidates with relevant skills and knowledge can apply.

• What is the focus of the role?
Clinical data programming, validation, and compliance in clinical trials.

Application Tips
• Highlight your SAS programming skills and projects.
• Mention knowledge of clinical data standards (GCDMP, CDISC).
• Include any internship or coursework related to clinical trials.
• Emphasize analytical and data handling skills.