Pharmacovigilance Professionals Wanted at Teva Pharmaceuticals – Bangalore

Teva Pharmaceuticals is hiring experienced Pharmacovigilance Professionals for their office in Bangalore, India (560052). With over 200 million people worldwide taking Teva’s medicines daily, this is your chance to contribute to global health.

Job Overview – Pharmacovigilance Professional

Location: Bangalore, India (560052)

Position: Pharmacovigilance Professional

Experience Required:

3-4 years in pharmacovigilance, including experience in Individual Case Safety Report (ICSR) processing and literature review.

Qualification:

• Any life sciences/pharmaceutical/healthcare professional graduate (B. Pharmacy, M. Pharmacy, Pharm D, BDS).
• Solid understanding of pharmacovigilance concepts, regulations, and procedures
• Advanced proficiency in Microsoft Office platforms
• Minimum of 02 to 04 years of experience in pharmacovigilance including literature review process in ICSR
• Experience in patient safety/pharmacovigilance: solid knowledge in pharmacovigilance concepts, regulations, and procedures.
• Advanced knowledge of Microsoft Office platforms.
• Flexible to adapt to shifting team priorities.
• Excellent communication skills including written, verbal, and non-verbal.
• Excellent Interpersonal and people skills. Good analytical skills and problem-solving skills.

Key Responsibilities:

As a Pharmacovigilance Professional at Teva Pharmaceuticals, you will:

• Processing serious & non-serious adverse events from various post-marketing sources.
• Ensure accurate and consistent medical coding through MedDRA (Medical Dictionary for Regulatory Activities) for all events in Safety Database.
• Data verification between source documents and entered data in Safety Database for evaluation of events/suspect drug coding, seriousness, causality, listedness and narrative writing.
• Evaluate the need for follow-ups, queries with various stakeholders for correct and accurate data transfer to various parties
• Ensure that quality data is analyzed for any trending and to prepare team for process stabilization.
• Providing administrative support by taking up complete responsibility of assigned case processing related activities on day-to-day basis.
• Coordinate with internal/ external stakeholders to obtain necessary information required for day-to­ day operations and to update the reporting manager on status reports on real time basis.
• Effective communications to be maintained with internal (related departments and units) & external (partners, authorities, vendors) stake holders in order to run the process as transparent as possible.

Pharmacovigilance Associate-Patient Safety Operations

• Perform the case processing and related activities in alignment with patient Safety Operations.
• Extensive knowledge of Medical Terminology, clinical pharmacology, patient treatment, diagnostic investigations & pathology.
• Exp in medical coding through MedDRA (Medical Dictionary for Regulatory Activities) for all events in safety database.

Pharmacovigilance Associate – Literature Review

• Relevant experience in Pharmacovigilance including Literature review process in ICSR Experience in Patient Safety/ solid
• knowledge in Pharmacovigilance concepts, regulations & procedures.
• Knowledge of database: Embase, Medline, Pubmed, Ovid, etc.
• Support PV teams like case processing, training teams, Quality assurance, audits & inspection etc

Teva Pharmaceuticals’ Equal Employment Commitment

Teva Pharmaceuticals is committed to diversity and equal employment opportunities. We ensure that employment decisions are made without regard to race, age, gender, disability, or any other legally protected status. We encourage candidates who require accommodations to apply and will provide support throughout the recruitment process.

How to Apply

Ready to take the next step in your career? Apply online for the Pharmacovigilance Professional role at Teva Pharmaceuticals via the link below:
Apply Here

Tagged as: Good Clinical Practice (GCP)