Instagram
youtube
Facebook

Statistical Data Sciences Lead (Ic)

8-12 years
Not Disclosed
10 July 28, 2025
Job Description
Job Type: Hybrid 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) – Chennai (Hybrid)

Job Summary:

Pfizer is seeking a highly productive and independent Statistical Data Sciences Lead (IC) to oversee statistical programming across clinical trials. This hybrid position, based in Chennai, is ideal for experienced professionals who want to make a lasting impact on global drug development by delivering top-tier datasets, tables, and clinical programming deliverables in alignment with Pfizer’s SOPs and regulatory standards.


Key Responsibilities:

  • Act as the programming point of contact at the study level and contribute to asset/submission-level deliverables.

  • Lead the delivery of high-quality datasets, tables, listings, and figures for clinical reports.

  • Manage programming strategy, resource planning, and timeline development in coordination with department leadership.

  • Oversee vendor/offshore programming support and perform hands-on programming as needed.

  • Ensure programming deliverables meet Pfizer standards and regulatory expectations.

  • Maintain complete documentation and Trial Master File compliance throughout the study lifecycle.

  • Collaborate with statisticians, programmers, and cross-functional teams to develop clear specifications.

  • Apply therapeutic area and safety data standards; assist in standards development.

  • Drive innovation by contributing to department-level initiatives and anticipating technical challenges.


Required Skills & Qualifications:

  • Strong experience in statistical programming within the pharmaceutical or clinical research industry.

  • Expertise in statistical software such as SAS and familiarity with data standards (e.g., CDISC, SDTM, ADaM).

  • Deep understanding of GxP, ICH-GCP, and regulatory compliance requirements.

  • Demonstrated ability to lead studies, manage vendors, and deliver critical programming outputs.

  • Strong analytical, problem-solving, and communication skills.

  • Experience with safety data and therapeutic area-specific standards.

  • Bachelor's or Master's degree in Biostatistics, Statistics, Computer Science, or related field.


Perks & Benefits:

  • Competitive compensation and benefits package.

  • Flexible hybrid work model supporting work-life balance.

  • Opportunity to work on a global drug development portfolio.

  • Career growth in a leading pharmaceutical organization.

  • Inclusive and collaborative work environment.

  • Access to training, leadership programs, and development resources.


Company Description:

Pfizer is a global biopharmaceutical leader focused on breakthroughs that change patients’ lives. With a cutting-edge R&D organization and a robust clinical pipeline, Pfizer is committed to delivering innovative medicines through scientific excellence and operational integrity.


Work Mode: Hybrid (Flexible Location – Chennai, India)


Call to Action:

Ready to lead high-impact clinical programming projects with a global pharmaceutical leader? Apply now to join Pfizer and contribute to life-changing innovations in healthcare.