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Syneos Health, a global biopharmaceutical solutions leader, is hiring a Statistical Programmer II in Hyderabad, India (Hybrid). This opportunity is ideal for professionals with 3–4.5 years of experience in SAS programming, ADaM dataset development, and clinical trial reporting.
If you’re passionate about clinical data, regulatory submissions, and making an impact in patient outcomes, this role offers a chance to accelerate your career in a global organization that has supported 94% of FDA novel drug approvals in the past five years.
Key Responsibilities
- Develop, validate, and maintain ADaM datasets in compliance with CDISC standards.
- Perform advanced SAS programming (Base SAS, SAS Macro, SAS SQL) for clinical trial analysis and reporting.
- Generate high-quality Tables, Listings, and Figures (TFLs) for safety and efficacy data.
- Collaborate with cross-functional teams to ensure accurate regulatory submissions.
- Support ISS/ISE preparation for submission packages.
- Contribute to PK/PD analysis and data integration for complex studies.
- Apply expertise in Oncology, Neuroscience, and Immunology therapeutic areas.
Required Qualifications
- Education: Bachelor’s or Master’s degree in Pharma, Statistics, Biostatistics, Computer Science, Life Sciences, or related field.
- Experience: 3–4.5 years in clinical trial SAS programming.
- Technical Expertise:
- Advanced SAS (Base SAS, Macro, SQL).
- ADaM dataset development and CDISC compliance.
- TFL generation (safety + efficacy).
- Good to Have:
- Programming patient narratives.
- Preparing ISS/ISE summaries.
- PK/PD data analysis.
Why Join Syneos Health?
- Opportunity to work on global clinical studies impacting millions of patients.
- Career growth through structured training and mentorship.
- Exposure to cutting-edge biostatistics and regulatory science.
- Hybrid work model for flexibility.
- Inclusive culture that values diversity, authenticity, and innovation.
Application Process
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