GPV Professional, Case Processing at TEVA Pharmaceuticals – Apply
Bangalore, India | Pharmacovigilance Jobs at Teva
ID: 70380
A rare chance has emerged for qualified professionals to join Teva Pharmaceuticals as a GPV Professional in Case Processing. Located in Bangalore, India, this pharmacovigilance career opportunity invites individuals with a strong background in drug safety and a passion for ensuring patient safety. Interested candidates are encouraged to apply promptly.
About the Company
Teva Pharmaceuticals is a leading innovative biopharmaceutical company, recognized for its world-class generics business. The organization is dedicated to addressing patients’ needs through innovation in fields such as neuroscience and immunology, while delivering high-quality medicines globally. Teva fosters a high-performing and inclusive culture that values collaboration and fresh thinking, providing employees with opportunities for growth and a balanced work-life experience.
Job Details:
- Position: GPV Professional, Case Processing
- Location: Bangalore, India
- Job ID: 70380
Job Description: GPV Case Processing
The GPV Professional will play a crucial role in processing serious and non-serious adverse events from various post-marketing sources. This position requires ensuring accurate medical coding and data verification, evaluating the need for follow-ups, and maintaining effective communication with stakeholders to facilitate transparent processes.
Key Responsibilities
- 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 the Safety Database.
- Data verification between source documents and entered data in the Safety Database for evaluation of events/suspect drug coding, seriousness, causality, listedness, and narrative writing.
- Evaluate the need for follow-ups and queries with various stakeholders for correct and accurate data transfer to various parties.
- Ensure that quality data is analyzed for any trends and to prepare the team for process stabilization.
- Providing administrative support by taking up complete responsibility of assigned case processing-related activities on a 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 a real-time basis.
- Effective communication to be maintained with internal (related departments and units) & external (partners, authorities, vendors) stakeholders in order to run the process as transparent as possible.
- Assist in Safety Database-related administrative and procedural activities as required or requested and to ensure that all assigned tasks are performed in compliance with the work instructions and GVP modules.
- Ensure that the quality of case processing and assigned tasks are evaluated and trends are identified for process improvement.
- Various compliance metrics like case timelines, assigned trainings, and TAT for assigned activities are met.
- Provide analytical support to peers and managers for investigations & analysis of various trends as a part of audits and inspections.
- Mentoring/Training the new hires with case processing knowledge transfer, evaluating their progress close to perfection during their initial phases of learning curves.
Eligibility for Pharmacovigilance Jobs
- M.Pharm, Pharm D, B.Pharm, BDS education.
- Extensive knowledge of medical terminology, clinical pharmacology, patient treatment, diagnostic investigations, and pathology.
- Sound knowledge of pharmacovigilance principles and international regulatory requirements related to drug and patient safety.
- Basic knowledge of the TEVA product portfolio, its therapeutic areas expertise, mechanism of action, and its product/patient safety index.
- Possess excellent communication skills with professional English speaking, writing, and presenting skills and must be detail-oriented.
How to Apply
Interested candidates can apply through the following link:
CLICK HERE FOR THE ORIGINAL NOTIFICATION / APPLY ONLINE
This opportunity at Teva Pharmaceuticals offers a chance to contribute significantly to patient safety and pharmacovigilance. For professionals seeking pharmacovigilance jobs, it offers an opportunity for professional growth and impact in the biopharmaceutical field. Qualified candidates are encouraged to review the original notification and apply promptly.
