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Data Manager, Clinical Data Sciences

Pfizer
Pfizer
0-2 years
3-5 LPA
Chennai, India
8 April 27, 2026
Job Description
Job Type: Full Time Education: B.Pharm, M.Pharm, Pharm D., BSc., MSc. Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Data Manager – Clinical Data Sciences


Location: Chennai, India (On-Premise)
Company: Pfizer
Job Type: Full-Time
Job ID: 4954891
Experience Required: 2–5 years (Freshers not eligible)


About the Company
Pfizer is a globally recognized leader in biopharmaceutical innovation, committed to advancing breakthrough therapies that transform patient lives. With a strong presence in clinical research and drug development, Pfizer continues to set benchmarks in data-driven healthcare solutions.


Job Overview
The Data Manager – Clinical Data Sciences is a key contributor within the Clinical Data and Information Sciences (CDIS) team under Clinical Development & Operations. This role focuses on ensuring high-quality clinical data management, supporting global clinical trials, and maintaining data integrity across the Pfizer portfolio.


Key Responsibilities

  • Serve as Data Manager for one or more clinical trials with minimal supervision

  • Lead end-to-end clinical data management activities including data collection, validation, and cleaning

  • Design and manage clinical databases, including CRF and non-CRF data collection tools using EDC systems

  • Develop, maintain, and execute Data Management Plans (DMP)

  • Perform ongoing data review and query management to ensure data accuracy and completeness

  • Collaborate closely with Clinical Data Scientists to drive operational excellence

  • Generate and analyze Data Management metrics and reports

  • Ensure timely database release and support submission-related activities

  • Maintain high-quality documentation in Trial Master File (TMF) aligned with regulatory expectations

  • Ensure compliance with SOPs, GCP guidelines, and global regulatory standards


Required Qualifications

  • Bachelor’s or Master’s degree in Life Sciences, Pharmacy, Biotechnology, or related field

  • 2–5 years of experience in Clinical Data Management or related domain

  • Hands-on experience with EDC systems, CRF design, and clinical databases

  • Strong understanding of clinical trial processes, CDISC standards, and data integrity principles

  • Familiarity with ICH-GCP guidelines and regulatory compliance requirements

  • Excellent analytical, problem-solving, and communication skills


Work Environment

  • On-premise role based in Chennai, India

  • Collaborative environment within global clinical development teams


Why This Role Matters
This position plays a critical role in ensuring the accuracy, reliability, and regulatory compliance of clinical trial data, directly impacting drug development outcomes and patient safety on a global scale.


Important Note for Applicants
This is a mid-level role requiring prior experience in Clinical Data Management. Freshers are advised to apply for entry-level roles such as Clinical Data Coordinator or Clinical Trial Assistant before targeting this position.


How to Apply
Interested candidates can apply through the official careers page of Pfizer or explore similar global opportunities on ThePharmaDaily.com for verified pharma and clinical research jobs.