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Regulatory Affairs Associate Director - UK, Biotech

This job is no longer available

Employer
Meet Recruitment
Posted
Thursday, July 26, 2012
Closes
Thursday, August 23, 2012
Ref
RA-ADcae
Location
South East England - more information on application
Contract Type
Permanent
Hours
Salary
range based on experience, great bonus and benefits

Further information

Regulatory Affairs, Manager, Associate Director, Regulatory Submissions, Regulatory Agencies Representative, Regulatory Line Manager, AD RA, Global Regulatory

Please note: the Client can only accept applications from candidates with working rights inside the EU

The client is a rapidly growing Biotech, HQ in America, 20 years of experience across oncology, cardiology and infectious diseases.

A fantastic role, ideal for a Regulatory Affairs Manager looking to take a step forward in their career. This new role will be sought after, so do not hesitate to call today!

This position as Associate Director of Regulatory Affairs will offer you full responsibility for all EU Regulatory Submissions, global interaction, provide guidance to development teams and represent the company to Regulatory Agencies.

Salary: £65,000 - £75,000 + a great bonus

Location: office based role, South East England

More information on application.

Working as the Associate Director / Manager of Regulatory Affairs your responsibilities will include:

  • Guidance on regulatory decisions and agency interaction
  • Strategy across regulatory submissions along scientific and technical reviews
  • Represent the company with regulatory agencies
  • Line management of EU regulatory staff – performance review, training and appraisals

To be successful in this process, you must have the following expertise:

  • Background in Regulatory Affairs – ideally to manager or director levels
  • 8yrs+ in clinical, RA or QA ideal
  • European or Global scope and responsibilities

You must have the following academic/skills set:

  • Strong life sciences education
  • Previous line management experience beneficial
  • Fluent English

Full company details and job description are available upon application; no CV is submitted until full discussion has taken place. Please contact Craig Edwards at Meet on +44 203 178 7488 or email craig@peoplewithchemistry.com

Contact me via LinkedIn at the following link: http://uk.linkedin.com/in/craigedwardsmeet

Find out more about Meet at www.peoplewithchemistry.com

Meet are good people who are great at recruitment for Pharma positions. We're proud to partner with the industry's leading CROs, Pharmaceutical and Healthcare companies -helping them find and secure the best global talent available

Associated keywords: Pharmaceutical, Biotech, Biotechnology, Biochemistry, CRO, Pharma, Pharmaceutical, Clinical, Clinical Regulatory Affairs, Associate Director, Director, Manager, Submissions, GRA, RA, Regulatory Affairs, Regulatory Submissions, Regulatory Manager, Regulatory Affairs Director, Regulatory Affairs Associate Director, Regulatory Line Management, UK, England, South-East, Surrey, Berkshire, Buckinghamshire, West Sussex area,

Regulatory Affairs, Manager, Associate Director, Regulatory Submissions, Regulatory Agencies Representative, Regulatory Line Manager, AD RA, Global Regulatory - Ideal for a Regulatory Manager to take a step forward in their career to AD level

Meet Recruitment


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