Job Title: Senior Associate, Data Manager – Clinical Data Sciences
Company: Pfizer
Location: India – Chennai
Department: Clinical Data and Information Sciences (CDIS)
Job ID: 4952888
Employment Type: Full-Time
Experience Required: Minimum 3–5 years of experience in clinical data management, clinical trials, or related pharmaceutical/biotech data management roles.
About Pfizer
Pfizer is a global biopharmaceutical company committed to delivering breakthroughs that transform patients’ lives. Our Research & Development teams drive innovation to bring life-changing medicines and medical solutions to the world. Pfizer fosters a culture of purpose, collaboration, and scientific rigor, enabling employees to contribute meaningfully to global health initiatives.
Role Overview
As a Senior Associate, Data Manager within the Clinical Data and Information Sciences (CDIS) group, you will oversee the collection, review, and integrity of clinical trial data across Pfizer’s portfolio. You will be responsible for executing critical data management deliverables, ensuring compliance with regulatory standards, and supporting high-quality clinical data to enable robust decision-making.
Key Responsibilities
Clinical Data Management
Serve as Data Manager for one or more clinical trials with minimal supervision, overseeing CDIS activities including database design, data acquisition standards, and testing of clinical data collection tools (CRF and non-CRF) using EDC systems or other data collection platforms.
Develop and maintain study-specific Data Management Plans (DMP) and ensure timely, high-quality documentation.
Conduct proactive data review, query management, data cleaning, and ensure data integrity across all study datasets.
Collaborate with Clinical Data Scientists to monitor operational excellence across all CDIS deliverables.
Regulatory and Compliance
Ensure work is performed in accordance with applicable SOPs, regulatory requirements, and Pfizer working practices.
Maintain high-quality study-specific CDIS documents in the Trial Master File (TMF) to support inspection readiness and regulatory submissions.
Facilitate database release and submission-related activities in compliance with global standards.
Data Visualization & Reporting
Provide data access, visualization, and metrics reporting to support study teams and decision-making.
Support the preparation of reports and dashboards to track study progress, query resolution, and data quality metrics.
Operational Excellence
Collaborate across CDIS teams to implement standards, ensure consistent data collection practices, and optimize data management workflows.
Identify and implement process improvements to enhance data quality, efficiency, and compliance.
Serve as a point of contact for cross-functional teams regarding data management activities and system functionalities.
Educational Qualifications
Bachelor’s or Master’s degree in Life Sciences, Pharmacy, Clinical Research, Health Informatics, or a related field.
Skills & Competencies
Hands-on experience with EDC systems, data acquisition tools, and clinical trial data standards.
Strong knowledge of query management, data cleaning, and clinical database processes.
Familiarity with regulatory requirements, Good Clinical Practice (GCP), and Trial Master File (TMF) documentation.
Excellent analytical, organizational, and communication skills.
Ability to manage multiple priorities and deliver high-quality outputs in a fast-paced environment.
Why Join Pfizer?
Pfizer offers a collaborative and innovative environment where your expertise in clinical data management will directly impact the delivery of safe and effective medicines worldwide. You will contribute to global clinical programs, ensure data integrity for regulatory submissions, and play a critical role in advancing patient-centric research.
Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.
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