Teva Pharmaceutical Industries, a global leader in generic and biopharmaceutical medicines, is seeking talented candidates for the role of Pharmacovigilance Associate in its Patient Safety Operations team.
Job Description
The responsibilities include:
- Processing serious and non-serious adverse events from post-marketing sources.
- Ensuring accurate medical coding via MedDRA for events in the Safety Database.
- Verifying data between source documents and the database, focusing on seriousness, causality, and narrative writing.
- Coordinating follow-ups and queries with stakeholders for accurate data transfer.
- Analyzing data trends to enhance process stabilization and prepare reports.
- Maintaining communication with internal and external stakeholders to ensure smooth operations.
- Supporting database-related administrative tasks and ensuring compliance with GVP guidelines.
- Training and mentoring new hires in case processing activities.
Candidate Profile
Qualification:
- M.Pharm, Pharm.D, or BDS postgraduate in registered life sciences.
Experience:
- 2 to 4 years of experience in pharmacovigilance case processing or related activities.
Skills:
- Knowledge of safety databases and regulatory requirements.
- Excellent communication and analytical skills.
- Experience with MedDRA coding and patient safety operations.
Additional Details
- Location: Bangalore, India
- Industry Type: Pharma/Healthcare/Clinical Research
- Functional Area: Regulatory Affairs
- Application End Date: 20th December 2024
How to Apply
Interested candidates with the requisite qualifications and experience can apply before the deadline.