Senior Manager Regulatory Affairs in Uxbridge

20 Nov 2018
18 Dec 2018
Regulatory Affairs
Contract Type
Laura Durrell at CK Clinical is recruiting for a Senior Manager 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:
- Contributes to development of EU regulatory product strategy.
- Ensure that the strategy and deliverables are aligned with the company's goals.
- Maintain awareness of all emerging issues and how they could impact the strategy.

Further responsibilities will include:
- Responsible for building regulatory dossiers to agreed timeline.
- Liaise with regulatory franchise team and other stakeholders.
- Managing and developing staff.

Your Background:
To succeed in this role, you will come from a background in:        
- Bachelors degree in scientific discipline.
- Extensive experience in regulatory affairs and EU centralised procedure.
- In depth understanding of CTD modules: non-clinical, CMC and Clinical.

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 CL43967 in all correspondence.

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