Associate Data Manager – Clinical Data Sciences
Company: Pfizer
Job Requisition ID: 4960826
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 Associate Data Manager, Clinical Data Sciences, is responsible for ensuring timely, accurate, and high-quality clinical data review and query management activities supporting Pfizer’s clinical development portfolio.
The role focuses on execution of clinical data management deliverables, maintaining data integrity, supporting electronic data capture systems, and ensuring compliance with clinical data management standards and regulatory requirements.
Key Responsibilities
Clinical Data Review & Query Management
Perform clinical data review activities to ensure accuracy, completeness, and consistency of clinical trial data.
Manage and resolve data queries to support clean and reliable clinical databases.
Support proactive data review, data cleaning, and quality monitoring activities.
Ensure clinical data integrity throughout the study lifecycle.
Clinical Database Design & Management
Assist in clinical database development activities including:
Database design documentation
Testing and validation
Implementation of clinical data collection tools
Support configuration and management of:
Electronic Data Capture (EDC) systems
CRF (Case Report Form) and non-CRF data collection tools
Other clinical data collection systems
Clinical Trial Documentation & Compliance
Maintain study-specific Clinical Data Sciences (CDIS) documentation within the Trial Master File (TMF).
Ensure documentation quality and timely filing to support:
Regulatory inspections
Submission readiness
Audit compliance
Perform activities according to applicable SOPs, guidelines, and working procedures.
Operational Excellence & Cross-functional Collaboration
Collaborate with Data Managers and Clinical Data Scientists to support:
Data acquisition processes
Data review strategies
Query management
E-data processing
Data access and visualization
Data management metrics reporting
Database release activities
Regulatory submission support
Support implementation of clinical data management standards and best practices.
Required Experience
1–3 years of experience preferred in Clinical Data Management, Clinical Research, or related pharmaceutical/biotechnology roles.
Experience with clinical trial data review, query management, or EDC systems preferred.
Understanding of clinical research processes, data standards, and regulatory requirements.
Experience working with clinical databases, CRFs, and clinical data management workflows is desirable.
Required Skills & Competencies
Knowledge of clinical data management principles and processes.
Ability to review and analyze clinical trial data.
Understanding of EDC systems and electronic clinical data workflows.
Strong attention to detail and commitment to data quality.
Ability to work collaboratively with cross-functional clinical teams.
Good documentation and organizational skills.
Knowledge of SOP compliance and regulated clinical environments.
Educational Qualification
Preferred Qualifications:
Bachelor’s or Master’s degree in:
Life Sciences
Pharmacy
Biotechnology
Clinical Research
Healthcare Sciences
Related scientific disciplines
Experience Level
Preferred Experience: 1–3 years in:
Clinical Data Management
Clinical Data Sciences
Clinical Research Operations
Electronic Data Capture (EDC) systems
Pharmaceutical/Biotech clinical trials
Suitable Profiles:
Associate Data Manager
Clinical Data Associate
Clinical Data Coordinator
Clinical Research Associate (CRA) with data management exposure
Clinical Data Management Executive
Salary Package (Market Estimate)
Estimated CTC: ₹6–12 LPA (based on Indian Clinical Data Management market standards, experience, qualification, and company benchmarks. Official JD does not specify salary.)
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