Associate Director Regulatory Affairs-Maidenhead

CK Clinical
15 Apr 2017
15 May 2017
Contract Type
Full Time
Oliver Care is recruiting for an Associate Director Regulatory Clinical Trials to join a company in the Pharmaceutical industry at their site based in Maidenhead on a permanent basis.

The main purpose of the role will be to:
- Provide strategic regulatory expertise for clinical trials
- Be responsible for the delivery of global strategic regulatory advice to study teams
- Develop internal working procedures for global activities

Further responsibilities will include:
- Leadership of up to 6 direct reports, these include permanent and contract workers
- Ensuring all Regulatory CTA activity is completed as necessary
- Representing the regulatory function at a global level both internally and externally

In order to be considered for this role, you will be required to have the following qualifications, skills and experience:
- Extensive regulatory clinical trial experience, ideally with 6 sigma
- Excellent communication, leadership and time management skills
- Educated to degree level or equivalent experience

This is an excellent opportunity to join an ambitious, family first, global pharmaceutical company.

Benefits include a salary of up to £90k and a car allowance of over £7k.

CK Clinical 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 CL38769 in all correspondence.