Manager – Clinical Data Scientist
Company: Pfizer
Job Requisition ID: 4960825
Location: Chennai, India
Work Mode: On-site
Employment Type: Full-time
Function: Clinical Data & Information Sciences (CDIS)
Department: Clinical Development & Operations (CD&O)
Job Summary
The Clinical Data Scientist is responsible for representing Clinical Data & Information Sciences (CDIS) at the clinical study team level and leading all CDIS activities associated with clinical trials.
The role ensures high-quality clinical data delivery, adherence to data standards, inspection readiness, and operational excellence throughout the clinical trial lifecycle. The Clinical Data Scientist provides leadership and oversight to Data Managers while collaborating with cross-functional teams to support successful clinical development programs.
Key Responsibilities
Clinical Data Strategy & Study Leadership
Serve as Clinical Data Scientist for one or more clinical trials.
Own and oversee all CDIS deliverables, including:
Data acquisition standards
Data Management Plans (DMP)
Quality Risk Indicators (QRIs)
Third-party study data due diligence
Provide strategic input for clinical data collection, processing, analysis, and reporting.
Ensure delivery of high-quality clinical datasets within study timelines.
Cross-functional Collaboration & Operational Excellence
Act as a core member of the Clinical Study Team and collaborate with:
Research teams
Business units
Clinical operations teams
External data/service providers
Internal CDIS stakeholders
Drive operational excellence through implementation of CDIS best practices.
Provide technical expertise on:
Clinical data acquisition
Data processing workflows
Data consumption and reporting strategies
Data Quality Management & Compliance
Ensure quality and timely completion of all CDIS deliverables supporting clinical trials.
Maintain compliance with:
Standard Operating Procedures (SOPs)
Regulatory requirements
Global Clinical Data Management Practices (GCDMPs)
ALCOA data integrity principles
Ensure study-specific CDIS documentation within the Trial Master File (TMF) is complete, accurate, and inspection-ready.
Team Leadership & Resource Management
Provide leadership, guidance, and oversight to Data Managers supporting clinical trials.
Coordinate CDIS resources to ensure successful study execution.
Support team members in achieving quality, compliance, and operational objectives.
Work with Asset Leads to establish:
Study strategy
Timelines
Resource requirements
Clinical Trial Inspection Readiness
Ensure clinical data processes and documentation meet regulatory inspection requirements.
Drive proactive quality management throughout the study lifecycle.
Identify opportunities to improve efficiency, data quality, and clinical development outcomes.
Required Experience
5–8 years of experience preferred in Clinical Data Management, Clinical Data Sciences, or related pharmaceutical/biotechnology clinical research roles.
Strong experience managing clinical trial data and leading CDIS/Data Management activities.
Experience with:
Data Management Plans
Clinical database management
Data standards implementation
Risk-based quality management
Clinical trial inspection readiness
Experience providing leadership and oversight to clinical data management teams.
Required Skills & Competencies
Strong understanding of clinical development processes and clinical data workflows.
Expertise in clinical data standards and regulatory requirements.
Strong knowledge of:
EDC systems
Clinical data review processes
Data quality management
Data integrity principles
Excellent leadership, communication, and stakeholder management skills.
Ability to manage multiple priorities and deliver results within timelines.
Strong analytical, problem-solving, and decision-making abilities.
Ability to collaborate effectively with global cross-functional teams.
Educational Qualification
Preferred Qualifications:
Master’s degree or Bachelor’s degree in:
Life Sciences
Pharmacy
Biotechnology
Clinical Research
Healthcare Sciences
Related scientific disciplines
Experience Level
Preferred Experience: 5–8+ years in:
Clinical Data Management
Clinical Data Sciences
Pharmaceutical Clinical Trials
Clinical Operations
Data Standards and Regulatory Compliance
Suitable Profiles:
Clinical Data Scientist
Senior Clinical Data Manager
Lead Clinical Data Manager
Clinical Data Management Lead
CDIS Lead
Clinical Data Operations Manager
Salary Package (Market Estimate)
Estimated CTC: ₹18–30 LPA (based on Indian pharmaceutical clinical data management market standards, leadership experience, technical expertise, and company benchmarks. Official JD does not specify salary.)
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