Job Posting: Pharmacovigilance Associate II at Teva Pharmaceuticals
About Teva Pharmaceuticals
At Teva Pharmaceuticals, we are committed to making good health more affordable and accessible, helping millions worldwide lead healthier lives. As the world’s leading manufacturer of generic medicines and a producer of numerous products on the World Health Organization’s Essential Medicines List, we reach over 200 million people daily. Join us as we continue to make a difference with new ideas and innovative solutions.
Position Details
- Position Name: Pharmacovigilance Associate II
- Organization: Teva Pharmaceuticals
- Location: Bangalore, India, 560052
- Salary: ₹17.6 Lakhs per year
- Experience: 5-6 years
- Qualification: B.Pharm, M.Pharm, Pharm.D, Lifesciences
Responsibilities
| Task | Description |
|---|---|
| Compliance | Ensure team activities comply with industry standards, company policies, and SOPs through procedural updates and training. |
| Strategy Development | Participate in building strategies for global pre-authorization studies and define and execute Teva standards. |
| Medical Evaluation | Perform medical evaluations and clarifications of clinical trial-related adverse events (AE) including narrative content, queries, coding, expectedness, seriousness, and causality with company summary/medical assessment as applicable. |
| Consultation | Act as a consultant or Single Point of Contact (SPOC) for case-related activities, maintaining a knowledge repository of process updates and changes in real-time. |
| Safety Review | Provide aggregate reviews of safety information, including clinical data, to maintain oversight of Teva’s medicinal products’ safety profile. |
| Administrative Support | Assist in V-Safe related administrative and procedural activities, ensuring all tasks are performed in compliance with work instructions and GVP modules. |
| Data Analysis | Ensure quality data analysis for trending and prepare the team for process stabilization. |
| Regulatory Compliance | Follow internal reporting key performance indicators to ensure regulatory compliance. |
Qualifications
| Requirement | Description |
|---|---|
| Education | Graduation/Post-graduation in registered life sciences. |
| Experience | Minimum of 5-6 years in Pharmacovigilance in a Biopharmaceutical/CRO industry, including experience in a large international organization. |
| Special Skills | Experience with pre-marketing studies and clinical trial case processing is an asset. In-depth knowledge of international PV regulations. |