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.
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