Job Post: Associate Safety Data Management Specialist
Job Summary:
Are you a recent graduate with a B.Pharm, M.Pharm, or Pharm.D degree? Pfizer is seeking highly motivated and detail-oriented individuals to join our pharmacovigilance team in Chennai, India as an Associate Safety Data Management Specialist. This entry-level position offers an excellent opportunity to gain hands-on experience in drug safety data management using the ARGUS Safety database, providing a solid foundation for a career in clinical safety.
Job Summary
As an Associate Safety Data Management Specialist, you will be responsible for the processing and management of Individual Case Safety Reports (ICSRs) received from both clinical trials and post-marketing sources. This role is critical in ensuring the accuracy, compliance, and scientific integrity of drug safety reporting, adhering to global regulatory standards and Pfizer’s internal protocols.
Responsibilities:
- Process and evaluate the validity of safety cases within the ARGUS Safety Database.
- Perform duplicate checks and create new cases for ICSR submissions.
- Identify and assess adverse events for seriousness and causality.
- Apply medical coding for drugs and events using established global standards.
- Draft comprehensive and accurate narratives and follow-up reports.
- Ensure data accuracy, completeness, and adherence to Pfizer’s stringent safety protocols.
- Review processed cases to maintain technical and regulatory compliance.
Requirements:
- Education: Bachelor of Pharmacy (B.Pharm), Master of Pharmacy (M.Pharm), or Doctor of Pharmacy (Pharm.D) degree.
- Experience: This is a freshers only position. No prior work experience is required.
- Skills:
- Excellent analytical and problem-solving skills.
- Strong written and verbal communication skills.
- Ability to collaborate effectively within a team environment.
- Exceptional attention to detail and commitment to accuracy.
- A proactive approach to continuous learning and professional development.
Preferred Skills:
- Certification in Pharmacovigilance or Drug Safety.
- Working knowledge of medical terminology.
- Familiarity with global pharmacovigilance regulations (e.g., FDA, EMA).
- Publications or academic experience in clinical or pharmaceutical sciences.
Benefits of Working at Pfizer:
- Impactful Work: Contribute to a global leader in healthcare innovation and make a difference in patient safety.
- Technical Expertise: Gain hands-on experience with the industry-leading ARGUS Safety Database.
- Work-Life Balance: Enjoy a hybrid work model that promotes flexibility and well-being.
- Career Growth: Benefit from excellent opportunities for professional development and career advancement in pharmacovigilance.
- Inclusive Culture: Be part of a diverse and collaborative workplace that values every individual.
Work Location:
- Location: Chennai, India
- Work Mode: Hybrid (combining on-site and remote work)
How to Apply:
If you meet the qualifications and are excited about the opportunity to join our pharmacovigilance team, we encourage you to apply. Please submit your application through our online career portal using the following link:
[Application Link]
We look forward to receiving your application!