Associate Director Regulatory Affairs in Uxbridge

20 Nov 2018
18 Dec 2018
Regulatory Affairs
Contract Type
Laura Durrell at CK Clinical is recruiting for an Associate Director Regulatory Affairs to join a Pharmaceutical company at their site based in Uxbridge on a contract basis.

The Company:
A global biopharmaceutical company with a strong pipeline in oncology and immunology.

Uxbridge, easily commutable from London and the surrounding areas.

The Role:
The main purpose of the role will be to:
- Responsible for the development of EU regulatory product strategy.
- Accountable for the maintenance of regulatory strategy, identifying and overcoming potential issues.
-  Responsible for the preparation of regulatory dossiers.

Further responsibilities will include:
- Responsible for interactions with EMA and national regulatory bodies.
- Participate in cross-functional activities.
- Maintain knowledge of key EU regulatory guidance and procedures.

Your Background:
To succeed in this role, you will come from a background in: 
- Degree in a scientific discipline.
- Experience with European regulatory affairs.
- Experience with Haematology / Oncology.

Please note that your CV should show exact dates of employment (month and year) and any gaps of a month or more should be explained.

CK Group is an Equal Opportunities employer and welcomes applications from all who meet our selection criteria.

If you do not hear back from us within 5 working days of your application for this role, it means that on this occasion you have not been shortlisted for the next stage of the recruitment campaign. Entitlement to work in the EEA is essential.  Please quote reference CL43965 in all correspondence.

Similar jobs

Similar jobs