Company Info
Teva is a global pharmaceutical leader and the world's largest generic medicines producer, committed to improving health and increasing access to quality health solutions worldwide. Our employees are at the core of our success, with colleagues in over 80 countries delivering the world's largest medicine cabinet to 200 million people every day. We offer a uniquely diverse portfolio of products and solutions for patients and we've built a promising pipeline centered around our core therapeutic areas. We are continually developing patient-centric solutions and significantly growing both our generic and specialty medicines business through investment in research and development, marketing, business development and innovation. This is how we improve health and enable people to live better, healthier lives. Join us on our journey of growth!
Job Description
Teva Global Pharmacovigilance (PhV) Agreements team in Romania is hiring a Global PhV Agreements Associate, Pharmacovigilance Compliance located in Bucharest.
The Global PhV Agreements team is responsible for preparing and managing PhV Agreements (PVAs) with business partners (other pharmaceutical companies) worldwide and ensuring that the requirements for safety data (adverse event reports, periodic safety update reports etc.) exchange are fulfilled and implemented in the Teva Pharmacovigilance System.
The responsibilities as Global PhV Agreements Associate, Pharmacovigilance Compliance mainly consist of:
• Initiate, develop, and negotiate PhV Agreements (PVAs) based on existing templates
• Review and update PVAs as necessary
• Update PVA templates and procedures
• Train and advise local safety officers in negotiating local PVAs and any other PVA related issues
• Maintain and update the PhV Agreements Management System
• Handling and answering inquiries (of partners or internal interfaces) received in the common mailbox
The ideal candidate should have:
• University background, at least first degree preferable in pharmacy, biosciences or law.
• Knowledge of pharmacovigilance is an asset
• Fluent in both written and spoken English
• Have good communication and cooperation skills
• Are motivated by working as a team player with significant interaction internally and externally
• Ability to maintain an overview and pay attention to details
• Have a structured approach to daily tasks and ability to maintain consistency
• A combination of being a quick learner, a person that enjoys being busy and a good sense of humor will qualify you to be our new colleague.
We are: A team of young, hard-working, open-minded and friendly colleagues
We offer:
• An exciting and challenging job in an innovative, flexible, and growing company
• Structured introduction according to training programs and standard operating procedures
Function
Regulatory Affairs
Sub Function
Pharmacovigilance
