Job Details

Senior Director, Regulatory Strategy Lead

4600
  • £250000
  • Durham, North Carolina, United States
  • Permanent

Now Hiring: Senior Director of Regulatory Affairs with a global CRO!

 

Are you looking for the next step in your career within Regulatory Affairs? If you have an in depth understanding of regulatory affairs within the pharmaceutical industry, particularly for Oncology products, this could be the role for you!

 

Overview:

Acting as a leader within the regulatory affairs strategy, you will provide guidance and advice on regulatory strategy for emerging biopharmaceutical clients, particularly focusing on drug development, product lifecycle and portfolio management within Oncology. Working within the frameworks of the US and European regulatory bodies, you will help to guide these clients to get products over the line!

 

Requirements:

  • Extensive background working in regulatory affairs, typically 15-20 years
  • Broad knowledge of the inner workings of EMA and FDA regulatory bodies, including with submissions and interactions
  • Relevant life sciences degree or equivalent experience
  • Analytical expert, with ability to manage multiple projects, clients and timelines to ensure success
  • Proven track record of meeting goals and deadlines within Reg Affairs
  • Prior experience within life sciences is essential, CRO experience is preferable

 

This role has an extremely competitive package, including fully remote work, unlimited annual leave and a salary range between $250k - 350k (DOE).

 

If this role sounds like it may interest you, please get in touch by applying below or reaching out at conor@warmanobrien.com

Conor Burke Consultant in Clinical Research

Apply for this role

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