Syngene International Ltd., a global leader in discovery and development research, is hiring an Executive – SAS Programmer for its Biometrics Division in Bangalore, India. This position offers an exciting opportunity for SAS-certified professionals with experience in clinical trials, CDISC, and pharmacokinetics to work with top pharmaceutical and biotech clients such as Bristol-Myers Squibb, Amgen, Baxter, and GSK.
If you’re passionate about programming, data integrity, and clinical research, this is your chance to make an impact in a world-class R&D environment.
🔍 Key Responsibilities
As an Executive – SAS Programmer, you will be responsible for:
- Reviewing study protocols and statistical analysis plans (SAP).
- Performing SAS programming for tables, listings, and graphs (TLGs).
- Developing CDISC-compliant SDTM and ADaM datasets.
- Supporting clinical trial deliverables from Phase I–IV.
- Collaborating with cross-functional biometrics and biostatistics teams.
- Performing validation and quality checks to ensure data accuracy.
- Supporting regulatory submissions and internal audits.
- Performing additional tasks as assigned by the organization.
🎓 Qualifications and Skills
Educational Requirements:
- M.Sc. in Life Sciences or equivalent field.
- SAS Programming Certification (mandatory).
Technical/Functional Skills:
- Proficiency in SAS and R programming (knowledge of Pinnacle 21 preferred).
- Experience in Clinical Trials, including Pharmacokinetics.
- Solid understanding of CDISC, SDTM, and ADaM standards.
- Strong documentation and data management skills.
Experience:
- 3–4 years of relevant experience in SAS programming and clinical data analysis.
Behavioral Competencies:
- Strong integrity, attention to detail, and English communication skills.
💼 Why Join Syngene?
- Work with world-class clients like BMS, Amgen, Merck KGaA, and Herbalife.
- Be part of a collaborative and innovative scientific community.
- Competitive compensation and benefits.
- Equal Opportunity Employer with inclusive workplace policies.
- Exposure to cutting-edge research and regulatory projects.