Looking to start your career in clinical data management and SAS programming? Thermo Fisher Scientific is hiring for the role of CDM Programmer I (SAS) in India. This is a fully remote opportunity ideal for candidates with 0โ2 years of experience in clinical research, data management, or programming.
This role offers a strong entry point into the pharmacovigilance, clinical trials, and data science domain, making it highly relevant for life sciences, pharmacy, and IT graduates.
๐ Job Overview
- Role: CDM Programmer I (SAS)
- Company: Thermo Fisher Scientific
- Location: Bangalore (Remote โ Work From Home)
- Experience: 0โ2 Years
- Job Type: Full-Time
- Work Schedule: Monday to Friday
๐ง Key Responsibilities
As a Clinical Data Management Programmer, you will:
- Develop and manage clinical trial databases
- Perform data imports, validation, and quality checks
- Create and test data listings for clinical review
- Support data management activities and deliverables
- Work with SAS programming tools and RDBMS systems
- Collaborate with cross-functional teams in clinical projects
- Ensure compliance with GCP (Good Clinical Practices) and SOPs
- Assist in problem-solving and data discrepancy resolution
- Contribute to training materials and documentation
๐ Qualifications & Eligibility
To apply for this CDM Programmer I (SAS) job, candidates should have:
- Bachelorโs degree in:
- Pharmacy (B.Pharm / M.Pharm)
- Life Sciences
- Computer Science / IT / Biotechnology
- 0โ2 years experience in:
- Clinical data management
- SAS programming (preferred)
- Database systems (RDBMS knowledge)
๐ก Required Skills
- Strong analytical and problem-solving skills
- Basic knowledge of SAS or other programming languages
- Understanding of clinical trials and data management workflows
- Good communication and documentation skills
- Ability to manage deadlines and multitask
- High attention to detail and data accuracy
๐ฐ Salary (Estimated)
- โน3.5 LPA โ โน6.5 LPA (based on experience and skillset)
๐ Benefits of Working at Thermo Fisher Scientific
- Work with a global leader in clinical research
- Exposure to cutting-edge life sciences projects
- Strong learning environment in clinical data management
- Opportunity to build a career in pharmacovigilance and clinical programming
- Flexible remote working model
- Career growth in SAS programming and clinical analytics
๐ Why This Role is Important
The demand for clinical data management jobs in India is rapidly increasing due to growth in clinical trials, CROs, and pharmaceutical companies. This role provides hands-on exposure to:
- Clinical trial databases
- Regulatory compliance (GCP)
- Data validation and reporting
- SAS-based clinical programming
๐ฅ How to Apply
