Position: Pharmacovigilance Associate
Roles and Responsibilities:
1. Pharmacovigilance Associate I (Literature Review)
- Participate in literature review activities, designing and implementing comprehensive literature search strategies for specific products.
- Demonstrate experience in Patient Safety and a solid understanding of pharmacovigilance concepts, regulations, and procedures.
- Work with databases such as Embase, Medline, PubMed, Ovid, etc.
- Provide support to PV teams, including case processing, training, quality assurance, audits, and inspections.
2. Pharmacovigilance Associate I (Patient Safety Operations)
- Perform case processing and related activities in alignment with Patient Safety Operations.
- Exhibit extensive knowledge of medical terminology, clinical pharmacology, patient treatment, diagnostic investigations, and pathology.
- Utilize experience in medical coding through MedDRA (Medical Dictionary for Regulatory Activities) for all events in the safety database.
Qualifications and Experience:
- Educational Qualification: M.Pharm, Pharm.D, or BDS
- Experience: 2-4 years in pharmacovigilance or related fields
Job Location:
Teva Pharmaceuticals, Brigade Senate 1, Hebbal Kempapura, Bengaluru – 24
Walk-in Interview Details:
- Date: 14th December 2024 (Saturday)
- Time: 09:00 AM – 02:00 PM
- Venue: Teva Pharmaceuticals, Brigade Senate 1, Hebbal Kempapura, Bengaluru – 24
Key Skills:
- Proficiency in databases like Embase, Medline, PubMed, and Ovid.
- Strong understanding of pharmacovigilance principles and practices.
- Expertise in medical coding using MedDRA.
- Knowledge of clinical pharmacology, medical terminology, and diagnostic processes.