Michael Page Linkedin

Information:

  • This job has been filled.

Job Vacancy Details

| Email to a friend | Apply Back to search results

Senior Regulatory Affairs Manager

Pharmaceutical

South Coast

Permanent ⁄ £50000 - £60000

Updated May 14, 2012


Working as the number two to the Director of regulatory, you will play a key role inmanaging the regulatory cycle for the business unit.

Responsibilities will include:

• Influencing regulatory strategy for the business
• Acting as the regulatory lead in the preparation of documentation for regulatory submissions in different parts of the world
• Planning, executing and maintaining the Marketing Authorisation Applications globally.
• Supporting clinical trial applications as necessary.
• Managing the relationships internally between research & development and technical as well as externally with the marketing partners and regulatory CRO's across the globe.
• Managing a team of Regulatory Affairs Associates

Who we're looking for
To be considered for this role you will haveexperience of Marketing Authorisation Applications and maintenance. You will also also be competent with EU and US regulatory markets and procedures.

About our client
Our client is a niche Pharmaceutical business with a global coverage. Based on the South Coast, the Senior Regulatory Affairs manager is a key appointment

What's on offer
up to £65,000 basic

Michael Page Contact
For further info, apply or phone on 0113 388 9000.  Job Ref: 13205523
Your application will be sent to Richard Goodall.

Job Search

job type

time period

Keyword type

Submit your CV

Michael Page International plc, Registered in England, Company Number 3310225

Registered Office: Page House, 1 Dashwood Lang Road, Addlestone, Weybridge, Surrey, KT15 2QW