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Novotech Hiring Clinical Data Programmer I (SAS) – Apply Now
Novotech
Bangalore
Clinical Data Management
SAS Programming
Full-Time
🏢 About Novotech
Novotech is a globally recognized Contract Research Organization (CRO) specializing in clinical trials, regulatory consulting, and drug development services. The company works with pharmaceutical and biotechnology sponsors across Asia-Pacific, Europe, and North America to accelerate clinical development and regulatory approvals.
📌 Job Overview
- Position: Clinical Data Programmer I (SAS)
- Company: Novotech
- Location: Bangalore, Karnataka
- Department: Clinical Data Management
- Employment Type: Full-Time
- Job ID: 3756
🔬 Key Responsibilities
- Develop and maintain SAS programs for clinical trial data.
- Support data cleaning, validation, and reporting activities.
- Generate clinical data listings and data extracts.
- Ensure compliance with Good Clinical Data Management Practices (GCDMP).
- Assist with database validation and discrepancy management.
- Collaborate with data managers, statisticians, and project teams.
- Maintain programming documentation and regulatory compliance.
- Support database lock preparation and data integrity checks.
🎓 Eligibility Criteria
- Bachelor’s or Master’s degree in Life Sciences
- Pharmacy (B.Pharm / M.Pharm)
- Biostatistics
- Computer Science or related fields
💻 Required Skills
- SAS programming knowledge
- Understanding of clinical data management processes
- Knowledge of GCDMP and clinical data standards
- Strong analytical and data validation skills
- Ability to work with cross-functional teams
⭐ Preferred Skills
- Experience with clinical trial data programming
- Knowledge of CDISC standards (SDTM / ADaM)
- Experience with EDC systems
- Understanding of clinical trial data validation
💰 Salary & Benefits
- Estimated Salary: ₹6 LPA – ₹9 LPA
- Health and wellness benefits
- Exposure to global clinical trials
- Professional training and certification support
- Career growth within Novotech
🎯 Interview Preparation Tips
- Understand clinical trial data structures
- Review SAS programming basics
- Learn CDISC standards (SDTM / ADaM)
- Understand clinical data validation workflows
Helpful learning resources:
📌 Note Before You Apply:
Kindly read the entire job description carefully before applying. Make sure your qualifications and experience align with the role requirements.
Kindly read the entire job description carefully before applying. Make sure your qualifications and experience align with the role requirements.
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