Sr. Statistical Programmer – Job Summary
Company: Syneos Health
Job Title: Sr. Statistical Programmer
Job ID: 25107604
Location: Remote (India)
Function: Biostatistics / Statistical Programming
Experience Level: Senior-Level Clinical SAS Programmer
Role Overview
The Sr. Statistical Programmer is responsible for developing, validating, and delivering clinical trial datasets, statistical outputs, tables, listings, and figures (TLFs) using SAS and other statistical programming tools. The role involves leading programming activities, ensuring regulatory compliance, mentoring junior programmers, and collaborating with biostatisticians, sponsors, and cross-functional clinical teams.
Key Responsibilities
Statistical Programming
Develop SAS programs for:
SDTM and analysis datasets
Tables, Listings, and Figures (TLFs)
Derived datasets and custom reports
Generate outputs according to Statistical Analysis Plans (SAPs) and programming specifications.
Perform validation programming and quality checks.
Study Deliverables & Documentation
Review and interpret:
Statistical Analysis Plans (SAPs)
Annotated CRFs
Mock Shells
Programming Specifications
Database Designs
Maintain complete and inspection-ready documentation.
Ensure compliance with SOPs, Work Instructions, ICH, and regulatory requirements.
Project Leadership
Act as Lead Statistical Programmer on assigned studies.
Coordinate programming activities and monitor deliverables.
Manage multiple studies and competing timelines.
Provide accurate effort estimation and project planning.
Team Collaboration
Work closely with:
Biostatisticians
Clinical Data Management Teams
Sponsors
Statistical Programmers
Participate in sponsor meetings, kickoff meetings, and bid defense activities.
Communicate project status, risks, and issues effectively.
Mentoring & Training
Guide and mentor junior programmers.
Review programming deliverables and provide technical feedback.
Develop and deliver internal training sessions.
Required Qualifications
Education
Bachelor's degree in:
Statistics
Mathematics
Computer Science
Life Sciences
Related Scientific Discipline
Equivalent combination of education and relevant experience may be considered.
Experience
Extensive SAS programming experience.
Strong experience in clinical trial statistical programming.
Experience leading programming activities on clinical studies.
Uttar Pradesh :
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Remote, India | Siliguri |Illinois :
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Europe | France | Latvia | Lendava | Leuven | Poland | Slovenia | Spain |Finland :
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Japan | Saitama |Tokyo :
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