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Statistical Programmer I

0-2 years
Not Disclosed
10 Sept. 24, 2025
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Statistical Programmer I – Syneos Health

Location: Gurugram, India
Job ID: 25101731
Updated: September 18, 2025


About Syneos Health

Syneos Health® is a fully integrated biopharmaceutical solutions organization focused on accelerating clinical development and improving patient outcomes.

  • Employees: 29,000 across 110 countries

  • Experience: Worked with 94% of Novel FDA-approved drugs, 95% of EMA-authorized products, 200+ studies, 73,000 sites, and 675,000+ trial patients.

  • Culture: Total Self culture fostering diversity, authenticity, career growth, and inclusion.


Job Overview

The Statistical Programmer I supports the Biostatistics and Statistical Programming team by creating, testing, and maintaining programs to support statistical analysis and reporting for clinical studies. This role works under the guidance of senior programmers and ensures compliance with project specifications, quality standards, and regulatory guidelines.


Key Responsibilities

Programming & Data Management:

  • Generate summary tables, data listings, graphs, and derived datasets per statistical analysis plans (SAPs) and programming specifications.

  • Perform validation programming and resolve discrepancies in collaboration with statisticians and project team members.

  • Ensure outputs meet project requirements and quality standards.

Collaboration & Communication:

  • Keep project team members informed of programming progress and issues.

  • Prepare for internal meetings, contribute ideas, and respect team input.

  • Assist with projects and initiatives as needed to support business goals.

Compliance & Documentation:

  • Follow SOPs, work instructions (WIs), and regulatory guidelines (e.g., ICH).

  • Maintain organized, up-to-date project documentation, verification, and quality control records.

  • Ensure documentation is inspection-ready.

Project Management:

  • Manage time and scheduling across multiple projects.

  • Adapt daily workload to priority changes or project timelines.

  • Complete programming tasks within allotted timeframes.

Other Duties:

  • Perform other work-related tasks as assigned.

  • Minimal travel may be required.


Qualifications & Requirements

  • Education: Undergraduate degree in a scientific or statistical discipline, or equivalent experience with demonstrated programming expertise.

  • Skills & Knowledge:

    • Proficiency in SAS or other statistical programming software

    • Understanding of clinical trial data and reporting standards

    • Excellent written and verbal communication skills in English

    • Ability to work independently and collaboratively in a team

  • Preferred Experience: Clinical trial environment experience is advantageous


Additional Information

  • Tasks and responsibilities may vary at the company’s discretion.

  • Equivalent experience or skills may be considered.

  • Commitment to diversity, inclusion, and ADA compliance.

  • Expressing interest adds you to Syneos Health’s talent pipeline for upcoming opportunities.