Job Description

My client, a CRO, is looking for a regulatory affairs executive, to act as a consultant, a specialist in the area, with particular experience within Toxicology and pre clinical OR CMC.

The role will involve your visiting clients and providing consultancy services on site in order that their projects are all compliant with Company Policy, standards and procedures.

Acting as the main point of liaison between company and client, you must have excellent communication and presentation skills.

Requirements for the position:-

A degree or equivalent in an appropriate discipline, for example Life Sciences, Pharmacy, Chemistry, Medicine, Veterinary Medicine.

A minimum of two years' experience in the pharmaceutical or pharmaceutical contract service industry or other appropriate experience.

For more information, please call Zoe on 01580 201616 or email your details to zoe.bennett@bluepelicanpharma.com

Regulatory affairs, regulatory, quality, project manager, project management.

Qualifications/Skills Required

N/A