Position: Senior Associate – Data Manager, Clinical Data Sciences
Location: India – Chennai
Job Type: Full-time
Job ID: 4943780
Posted: 29 Days Ago
Work Model: On-Premise
About Pfizer
At Pfizer, we’re in relentless pursuit of breakthroughs that change patients’ lives.
Every day, we innovate to make the world a healthier place.
Our purpose — Breakthroughs that change patients’ lives — is supported by a strong set of core values guiding both what we achieve and how we achieve it.
The Pfizer Research & Development (R&D) division serves as the core engine driving scientific innovation, powering the company’s mission to deliver life-changing medicines across the globe.
Pfizer also provides competitive compensation and comprehensive benefits tailored to meet the diverse needs of its global workforce.
Role Overview
The Senior Associate, Data Manager (Clinical Data Sciences) plays a key role within the Clinical Data and Information Sciences (CDIS) group — a core delivery unit within Clinical Development & Operations (CD&O).
This position is responsible for ensuring high-quality, timely clinical data management — including data review, query management, and maintaining the integrity of clinical trial data across Pfizer’s global portfolio.
The Data Manager will work collaboratively with Clinical Data Scientists to maintain operational excellence across all CDIS deliverables.
Key Responsibilities
Serve as the Data Manager for one or more clinical trials, working independently with minimal supervision.
Oversee end-to-end data management activities, including:
Selection and application of data acquisition standards.
Database design, including specification documentation and testing of clinical data collection tools (both CRF and non-CRF).
Execution of data review, data cleaning, and query management.
Management of data access, visualization, and metrics reporting.
Oversight of database release and submission-related activities.
Collaborate closely with the Clinical Data Scientist (CDS) to ensure consistency and quality across all CDIS deliverables.
Ensure that all activities adhere to Pfizer SOPs and regulatory requirements.
Maintain high-quality study-specific documentation in the Trial Master File (TMF), ensuring contemporaneous filing to support inspection readiness.
Drive operational excellence in collaboration with CDIS for data acquisition, proactive data review, e-data processing, and submission preparation.
Qualifications & Skills
Education: Bachelor’s degree (minimum requirement).
Experience: Demonstrated experience in clinical data management, preferably within global pharmaceutical or CRO environments.
Technical Skills:
Proficiency in Electronic Data Capture (EDC) systems and data visualization tools.
Strong understanding of data management standards, clinical trial processes, and regulatory requirements (e.g., ICH-GCP).
Core Competencies:
Excellent attention to detail and organizational skills.
Strong analytical and problem-solving abilities.
Effective communication and collaboration across cross-functional teams.
Ability to work independently with minimal supervision.
Work Environment
Assignment Type: On-Premise (Chennai, India)
Equal Opportunity Statement
Pfizer is an Equal Opportunity Employer and complies with all applicable equal employment opportunity laws in every jurisdiction where it operates.
We celebrate diversity and are committed to creating an inclusive environment for all employees.
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