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Senior Statistical Programmer (Clinical Pharmacology)

Syneos Health
Syneos Health
5-8 years
Not Disclosed
Gurgaon, India
1 May 8, 2026
Job Description
Job Type: Full Time Hybrid Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, mRS and EQ-5D-5L., Narrative Writing

Senior Statistical Programmer (Clinical Pharmacology)
Location: Gurugram (Hybrid)
Company: Syneos Health
Job ID: 25107869
Job Type: Full-Time
Industry: Biostatistics / Statistical Programming / Clinical Research / Clinical Pharmacology


About the Company

Syneos Health is a globally recognized and fully integrated life sciences organization focused on accelerating customer success across clinical development, medical affairs, and commercialization. The company collaborates with pharmaceutical, biotechnology, and healthcare innovators to support faster and more efficient drug development worldwide.

With more than 25,000 professionals globally, Syneos Health combines scientific expertise, operational excellence, and advanced analytics to deliver impactful healthcare and clinical research solutions.


Job Overview

Syneos Health is hiring experienced professionals for the role of Senior Statistical Programmer (Clinical Pharmacology). The selected candidate will be responsible for end-to-end statistical programming activities, including dataset generation, analysis reporting, validation programming, and clinical trial data support for clinical pharmacology and early-phase studies.

This opportunity is ideal for candidates with strong expertise in SAS programming, ADaM, SDTM, TFL generation, and clinical trial data analysis within pharmaceutical, CRO, or clinical research environments.


Key Responsibilities

  • Develop custom programming code using SAS or related statistical software
  • Generate:
    • Summary tables
    • Data listings
    • Graphs
    • Derived datasets
    • Statistical outputs
  • Perform end-to-end statistical programming activities according to Statistical Analysis Plans (SAPs) and programming specifications
  • Conduct validation programming and quality control checks to ensure data accuracy and compliance
  • Collaborate with Biostatisticians, Programmers, and cross-functional study teams to resolve discrepancies and programming issues
  • Maintain organized, inspection-ready project documentation and quality control records
  • Manage timelines and programming deliverables across multiple clinical studies
  • Develop dataset and output specifications based on sponsor and statistical requirements
  • Review:
    • Statistical Analysis Plans
    • Mock shells
    • Annotated CRFs
    • Programming specifications
    • SAS database designs
  • Lead programming activities for assigned projects and oversee junior programming team members
  • Participate in sponsor meetings, kickoff meetings, and bid defense discussions
  • Contribute to training, mentoring, and skill development initiatives for programming teams
  • Support process improvements and operational efficiency initiatives
  • Ensure compliance with:
    • ICH Guidelines
    • SOPs
    • Work Instructions (WIs)
    • Regulatory requirements

Required Qualifications

  • Undergraduate degree in:
    • Statistics
    • Biostatistics
    • Computer Science
    • Life Sciences
    • Mathematics
    • Or related scientific disciplines
  • Equivalent programming experience may also be considered
  • Strong understanding of:
    • Clinical trial data standards
    • Statistical programming workflows
    • Clinical pharmacology studies
    • Regulatory compliance requirements