Senior Regulatory Affairs Manager

Job Title: Senior Regulatory Affairs Manager
Contract Type: Permanent
Location: Stansted Mountfitchet, England
Salary: Competitive
Start Date: 2020-02-27
Reference: TS-18
Contact Name: Thomas Southgate
Contact Email:
Job Published: February 27, 2020 17:18

Job Description

Senior Manager - Regulatory Affairs
  • Excellent Salary and Package 
  • Outstanding Opportunity with a world-leading Pharmaceutical business
  • High profile role that will help shape regulatory strategy across a diverse product portfolio
We are currently helping a Global Pharmaceutical company to recruit for a Senior Regulatory Affairs Manager. This is a high-profile role for our client that will drive regulatory strategy across a number of key European Markets. 

The Company: 
Our client are a well-established Pharmaceutical business who have undergone some significant growth and development over the last 12 months. They have a large product portfolio that encompasses both Generic and Speciality drugs - supplied to a global customer-base.

The Role: 
The new Senior Regulatory Affairs Manager will be a key appointment for the business - operating at a Senior Level with key internal and external stakeholders within a global business. You will enjoy specific responsibility for:
  • Driving regulatory strategy throughout drug development phases; advising during development, approval and post-approval.
  • Preparing submissions to relevant Health Authorities across multiple jurisdictions 
  • Developing and communicating relevant regulatory strategies across a range of internal stakeholders
  • Influencing working processes across your area of expertise
The Candidate:
The successful Senior Regulatory Affairs Manager is likely to be working in a similar role at the moment; likely within a Pharmaceutical business. There are, however, some key capabilities that you will be able to demonstrate:
  • A higher-level qualification (Ph.D/Pharma.D, or MSc) in a relevant scientific or health care discipline is essential 
  • Excellent experience of development and approval stages - including regulatory pathways and regulations is essential 
  • An understanding and appreciation of the difficulties of a global Research and Development process - focused on Clinical Development, Benefit and Risk Assessments and Strategic positioning/labelling is essential 
If this opportunity sounds like it could be of interest, or to discuss it in more detail please don't hesitate to contact Tom Southgate @ NES Global Talent or hit apply to send your CV directly.

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