Senior Consultant Regulatory Affairs

Proclinical are recruiting on behalf of a leading consultancy organisation who have a vacancy for a Senior Consultant in Regulatory Affairs. In this role, you will be working for a company that offers excellent consulting services, with a dynamic and growing team of highly qualified consultants. This job offers an annual income of £65,000, and is based in High Wycombe.

Job Responsibilities:

• Providing a source of regulatory expertise in the development, registration and post-licensing activities of pharmaceutical products.
• Managing project teams and reviewing the work of junior personnel and company partners.
• Being responsible for management activities.
• Contribution to the functioning and business growth of the company.

Skills and Requirements:

• A graduate from a Pharmaceutical or Life Sciences subject, preferably with post-graduate qualification.
• At least ten years of experience in Regulatory Affairs, including a successful track record in the registration of medicinal products within Europe, especially in the UK and Ireland.
• A sound knowledge of pharmaceutical regulations and guidelines.
• Excellent written and verbal communication skills, with fluency in English

To Apply:

Please click on the Apply button. Please include a short note outlining why you are interested in the role and why you think you are suitable.

In case you have difficulty in applying or if you have any questions, please call Roberto Esposito on +44 203 761 5702 or upload your CV on our website - www.Proclinical.com.

A full job description is available on request.

Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.

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