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Manager, Clinical Data Scientist, Cdis

0-2 years
Not Disclosed
10 Sept. 15, 2025
Job Description
Job Type: Full Time Hybrid 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

Job Title

Manager, Clinical Data Scientist (CDIS)

Organisation

Pfizer Inc.

Location

  • Chennai, India

  • Full-time

  • Work Location Assignment: Hybrid

Job ID

4941343

Posted On

5 days ago


About Pfizer

  • Purpose: Breakthroughs that change patients’ lives through innovation every day.

  • Values: Clear expectations for what to achieve for patients and how to achieve them.

  • Research & Development: Core of Pfizer’s mission, advancing life-changing medicines.

  • Benefits: Competitive compensation and comprehensive benefits for diverse needs.

  • Culture: “Pfizer, We are One” – collaborative, inclusive, and patient-focused.


Role Summary

As part of the Clinical Data Sciences (CDS) group, within Clinical Development & Operations (CD&O), the Clinical Data Scientist (CDS) is responsible for high-quality and timely data management deliverables supporting Pfizer’s portfolio.

  • Provides strategies and services for effective use of internal and external data to advance R&D, commercialization, and precision medicine.

  • Designs, develops, and maintains deliverables used to collect, review, monitor, and ensure the integrity of clinical data.

  • Ensures quality study dataset release, application of standards, and consistency in asset/submission data.


Role Responsibilities

  • Act as Clinical Data Scientist & Trial Lead for one or more clinical trials, accountable for:

    • Data acquisition standards

    • Data Management Plan (DMP)

    • Quality risk indicators

    • Third-party study data due diligence

  • Serve as technical resource for study teams on Data Management (DM) and Risk-Based Monitoring (RBM) standards, tools, provisioning, and reporting.

  • Partner with Research Units, external DM vendors, and internal CDS staff to deliver high-quality data management.

  • Drive quality and efficiency to meet timelines and milestones, ensuring scientific and operational excellence.

  • Ensure all CDS-related work complies with applicable SOPs and working practices.

  • Participate in database design, documentation, testing, and implementation of clinical data collection tools (CRF & non-CRF) using EDC systems or other platforms.

  • Maintain and file high-quality study-specific CDS documents in the Trial Master File (TMF).

  • Ensure operational excellence across:

    • Standards application

    • Data acquisition & proactive review

    • Data integrity monitoring

    • Data cleaning & e-data processing

    • Data access, visualization, and database release


Qualifications & Skills

(Not explicitly listed in posting, inferred from responsibilities)

  • Strong knowledge of clinical data management principles

  • Experience with EDC systems, CRF/non-CRF tools

  • Familiarity with RBM, quality risk indicators, and data integrity practices

  • Ability to collaborate cross-functionally and with external partners

  • Strong organizational, documentation, and compliance focus


Equal Opportunity Statement

Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction where it operates.