PV Assiociate, Safety Surveillance Generics Team

at  Teva Pharmaceuticals

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PV Assiociate, Safety Surveillance Generics Team
Date: Jun 27, 2024
Location:Bucharest, Romania, 050713
Company: Teva Pharmaceuticals
Job Id: 56812

WHO WE ARE

Together, we’re on a mission to make good health more affordable and accessible, to help millions around the world enjoy healthier lives. It’s a mission that bonds our people across nearly 60 countries and a rich, diverse variety of nationalities and backgrounds. Working here means working with the world’s leading manufacturer of generic medicines, and the proud producer of many of the products on the World Health Organization’s Essential Medicines List. Today, at least 200 million people around the world take one of our medicines every single day. An amazing number, but we’re always looking for new ways to continue making a difference, and new people to make a difference with.

THE OPPORTUNITY

We are looking for a PV Associate who will contributes to the safety monitoring of all Teva pharmaceutical products, through technical and administrative support provided to Safety Scientists and Safety Physicians.
The PV Associate possesses very good analytical skills and performs medical and scientific data retrieval to support multiple activities (e.g. signal management, health hazard assessments etc.). The PV Associate works in collaborative manner with a cross-functional international team across multiple time zones, and operates well in a challenging environment and quickly adapts to shifting team and project priorities.

QUALIFICATIONS

• Bioscience background (student or graduate in: pharmacy, biology, veterinary medicine, nursing, paramedical studies).
• Experience in patient safety/pharmacovigilance: knowledge in pharmacovigilance concepts, regulations and procedures is an advantage.
• Advanced knowledge of Microsoft Office platforms.
• Proven ability to extract and collate information from various sources (e.g. organized data collection system), in specific formats
• Flexible to adapt to shifting team priorities.
• Fluent in English, spoken and written.

• Extracts reports from Teva’s global pharmacovigilance database and from the European pharmacovigilance database (EudraVigilance), used for preparing safety analyses, with the purpose of monitoring the safety profile of Teva pharmaceutical products.
• Monitors the requests for safety information received in the common designated mailbox, clarifies these requests, if needed, and performs a preliminary collection of the data necessary for answering these requests.
• Maintains a tracking system used to monitor the compliance of answers to such requests; archives all the necessary documentation in the designated archiving systems.
• Reviews the existing processes used for collection/retrieval of data and suggests ways to increase efficiency.
• Ensures a good communication and collaboration with other Teva departments, acting as a first contact point and offering initial clarifications about the contribution of the pharmacovigilance group to various types of common documents.
• Cooperates with other teams within the Medical Scientific Unit and other relevant groups within Teva Pharmacovigilance and other Teva departments (e.g. Medical Affairs, Quality Assurance, Regulatory Affairs).
• Prepares monthly and weekly reports used for signal management process.
• Performs all assigned tasks in line with relevant procedures.
• Performs other tasks assigned by the direct manager.