Regulatory Affairs Project Manager

Role: Regulatory Affairs Project Manager
Duration: 6 months
Location: South East, Surrey
Rate: £50 - £60p/h

The interim regulatory affairs project manager will be responsible for the management, strategic implementation and successful completion of drug and/or device development and commercialisation projects ensuring consistency and alignment with the company strategy, commitments, goals and values.

Throughout the six months the candidate will be responsible for:

- Marketing Authorisation Application (MAA)
- Routine Marketing Authorisation Maintenance (Variations/Renewals)
- Clinical Trial Applications (CTAs)
- General Regulatory Activities
- Regulatory Documentation Control
- General Activities

Qualifications/Requirements

- Life Science degree or relevant experience
- Experience in Regulatory Affairs and previous proven experience in managing the preparation of regulatory submissions

If this role is of interest to you then please don't hesitate to contact Peter Duvall at Real Staffing on 02077587322To find out more about Real please visit www.realstaffing.com