Sr Statistical Programmer(ADaM & TLF)
Syneos Health (company site, opens in a new tab)5–8 yrsHyderabadHybridDirect career pageEst. 12–20 LPA
Posted 20h ago
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Job description
Structured overview of role & requirements
About This Role
- Develop and validate SAS programming code to generate clinical trial summary tables, listings, graphs, and datasets per statistical analysis plans.
- Lead and monitor programming activities of other personnel, ensuring deliverables meet quality standards and timelines.
- Participate in project and sponsor meetings, prepare documentation, and mentor other programming staff.
Minimum Requirements
- 5-8 years of experience in SAS programming within clinical trial environments.
- Strong expertise in ADaM programming, specification writing, and TLF development, including Safety outputs.
- Undergraduate degree in scientific or statistical discipline or equivalent combined education and programming experience.
- Location: India - Remote or Hyderabad Hybrid; excellent English communication skills required.
Ideal Candidate Profile
- Experienced lead statistical programmer comfortable overseeing multiple projects and coordinating teams.
- Proficient in programming for Safety outputs and able to work independently on efficacy and late-phase clinical studies.
- Skilled in documentation, specification development, and effective cross-functional communication with sponsors and project teams.