Instagram
youtube
Facebook

Statistical Data Sciences Lead (Ic)

2+ years
₹25–35 LPA
10 Aug. 13, 2025
Job Description
Job Type: Full Time Education: B.Sc./M.Sc./B.Pharm/M.Pharm/Life science 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

Job Title: Statistical Data Sciences Lead (IC)
Location: Chennai, India
Employment Type: Full-time

About the Company:
Pfizer is dedicated to breakthroughs that change patients’ lives, with a mission to bring life-changing medicines to the world. Pfizer Research & Development serves as the driving force behind the company's innovative product pipeline.

Role Overview:
The Statistical Data Sciences Lead will be responsible for leading the delivery of analysis-ready datasets, tables, listings, and figures in line with Pfizer SOPs and processes. This role serves as the primary programming contact at the study level, with potential contributions at the asset/submission level.

Key Responsibilities:

  • Act as the programming lead ensuring excellence and adherence to high-quality programming standards.

  • Serve as the programming point of contact for assigned studies.

  • Oversee vendors and offshore support while also engaging in hands-on programming.

  • Collaborate with leadership and project teams to set strategy, timelines, and resource allocation for programming and analysis deliverables.

  • Ensure quality and timely delivery of datasets and displays for clinical study reports and other asset-level deliverables.

  • Maintain appropriate documentation and ensure proper Trial Master File filings.

  • Plan for all programmed deliverables, considering special data types and downstream uses of data.

  • Collaborate with statisticians and programming teams to ensure clear specifications are in place.

  • Apply knowledge of core safety and therapeutic area standards; contribute to the development of study-specific standards when needed.

  • Contribute to department-level initiatives.

  • Proactively identify and communicate potential issues to senior management.

  • Solve routine and complex programming-related problems.

Qualifications & Skills:

  • Extensive experience in statistical programming within clinical research.

  • Strong understanding of clinical data structures, statistical analysis, and reporting standards.

  • Ability to manage multiple priorities and deliver high-quality outputs within deadlines.

  • Excellent communication and leadership skills.

Work Location Assignment: Hybrid / Flexible

Estimated Salary: ₹25–35 LPA (Based on industry benchmarks for senior statistical programming roles in Chennai)