Pfizer, a global leader in pharmaceuticals, invites talented professionals to join our Worldwide Medical and Safety team as an Associate – Safety Data Management Specialist at our Chennai facility.
Posted on August 7, 2025, this full-time role offers a unique opportunity to contribute to evidence-based medical decisions, ensuring the safe and appropriate use of medicines for patients worldwide. Be part of our mission to empower healthcare through innovation and excellence.
About Pfizer
Pfizer is committed to advancing healthcare by delivering high-quality, evidence-based medical solutions. Our Chennai facility supports global safety data management, adhering to rigorous regulatory standards.
With a collaborative and inclusive culture, we provide a dynamic environment for professionals passionate about improving patient outcomes through robust safety processes.
Job Opportunity Details
We are seeking candidates with 1–2 years of experience for the Associate – Safety Data Management Specialist role. This hybrid position in Chennai offers a chance to grow with a global pharmaceutical leader.
- Job Title: Associate – Safety Data Management Specialist
- Job Requisition ID: 4939465
- Location: Chennai, India
- Work Model: Hybrid
- Application Method: Apply via Pfizer Careers
- Posted On: August 7, 2025
Role and Responsibilities
As a Safety Data Management Specialist, you will play a critical role in ensuring the safety and compliance of Pfizer’s medicinal products. Key responsibilities include:
- Case Processing: Review, rank, verify, and process case-related information, including event terms, validity, seriousness, and timelines.
- Case Assessment: Determine appropriate workflows and escalate complex cases with specific issues.
- Narrative Development: Write and edit case narratives for accuracy and clarity.
- Follow-Up Management: Perform case follow-ups and generate follow-up requests as needed.
- Quality Assurance: Review processed cases for accuracy, consistency, and compliance with regulatory requirements.
- Stakeholder Collaboration: Liaise with local and global partners for safety data collection and reconciliation.
- Regulatory Compliance: Ensure reportability of scheduled reports per global regulations and Pfizer policies.
- Knowledge Development: Maintain expertise in corporate regulations, SOPs, and safety database functions.
- Safety Activities: Participate in local, internal, and external safety-related initiatives.
Qualifications and Skills Required
Candidates must meet the following criteria to excel in this role:
Role | Qualifications | Experience | Key Skills |
---|---|---|---|
Safety Data Management Specialist | B.Pharm, M.Pharm, Pharm.D | 1–2 years | ICSR processing, ARGUS, medical terminology, regulatory compliance |
Minimum Requirements:
- Education: B.Pharm, M.Pharm, or Pharm.D.
- Experience: 1–2 years in end-to-end Individual Case Safety Report (ICSR) processing, including listedness assessment.
- Skills: Ability to work collaboratively in a team environment.
Preferred Requirements:
- Hands-on experience with the ARGUS safety database.
- Proficiency in processing XML source documents (E2B R2 and R3 formats).
- Strong knowledge of medical terminology and global drug safety regulations.
Why Join Pfizer?
Joining Pfizer offers numerous benefits to support your career and well-being:
- Career Growth: Access to professional development and global exposure.
- Innovative Environment: Work with cutting-edge safety data management systems.
- Inclusive Culture: Pfizer is an equal opportunity employer, fostering diversity and inclusion.
- Hybrid Work Model: Balance on-site and remote work for flexibility.
- Global Impact: Contribute to patient safety and healthcare decisions worldwide.
Why Chennai?
Our Chennai facility is located in a vibrant hub of India’s pharmaceutical industry, offering excellent connectivity and a dynamic work environment. Chennai’s thriving professional community and access to advanced technology make it an ideal location for career growth in safety data management.
How to Apply
Ready to make a difference? Apply for the Associate – Safety Data Management Specialist role via Pfizer Careers using the job requisition ID 4939465. Ensure your application includes an updated CV highlighting your qualifications and experience. For inquiries, visit Pfizer’s official website or contact the HR team through the careers portal.
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Application Process
- Step 1: Submit your application via Pfizer Careers with job ID 4939465.
- Step 2: Include your CV, detailing relevant experience and qualifications.
- Step 3: Await a response from Pfizer’s HR team for interview scheduling.
- Step 4: Successful candidates will be contacted for further steps and onboarding.
About Pfizer’s Commitment
Pfizer is dedicated to ensuring the safe and appropriate use of medicines through robust safety data management. Our Worldwide Medical and Safety team bridges evidence-based medical decisions with stakeholders, driving better health outcomes.
As an equal opportunity employer, Pfizer complies with all applicable employment legislation, fostering a diverse and inclusive workplace.
Take the Next Step
Don’t miss this opportunity to join Pfizer and contribute to global patient safety. Apply now for the Associate – Safety Data Management Specialist role in Chennai via Pfizer Careers. For more information, visit Pfizer’s official website. Your career in pharmaceutical safety starts here on August 7, 2025!