Description
World leading international Pharmaceutical client currently have a long term contract position for an experienced Regulatory Affairs Liaison.You will be responsible for the collection and presentation of product
registration data to ensure timely registration of new products, new indications and the renewals of established products.
- You will provide regulatory input to the therapeutic project teams located at product development sites.
- You will interact with European subsidiary regulatory managers in the execution of regulatory strategies and drug registration activities.
- You assist subsidiary personnel by providing scientific support.
- You will identify and track changes/trends in the medical practice and attitudes within European countries that might impact product and project responsibilities.
Profile
- You have a bachelor`s or a Master`s degree preferred
- Strong experience in regulatory affairs.
- We are looking for someone with excellent communication skills in English, both oral and written.
Experience in an international RA environment and knowledge of EU regulations are a must!
This is an exciting opening to work in dynamic team in a contract opportunity offering competitive rates of pay. Please apply now at or on for more information.