Life Sciences Pharmaceuticals
CY Partners have an exciting opportunity for a Regulatory Associate to come and join a leading global pharmaceutical, based at their site in Hertfordshire.
As a Regulatory Associate you will assist in the preparation of the nonclinical content for various global regulatory dossiers, working with their mature portfolio’s. Within this role, your responsibilities will include assisting in the preparation of nonclinical regulatory dossiers and completing timely and accurate regulatory dossiers for the approval and maintenance of product marketing and clinical trials applications.
Additional skills which would be desirable for this role include the following:
- Excellent capability in managing a fast paced, changing environment.
- Excellent written and verbal communication skills.
- Experience in data gathering/ information from a range of sources.
- An Understanding of pharmacology, pharmacokinetics & toxicology related to drug development.
Previous knowledge and some experience of regulatory affairs would be an advantage. This is an exciting opportunity and we look forward to receiving your application.
For a confidential chat about the role, contact us on 0191 477 4733 or email your CV across to [email protected]