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Regulatory Strategy Project Lead

Regulatory Strategy Project Lead

Job Title: Regulatory Strategy Project Lead
Contract Type: Permanent
Location: Worthing
Industry:
Salary: Industry leading salary and benefits
Start Date: 2020-03-11
Reference: V-46120
Contact Name: Jake Thomas
Contact Email: jake.thomas@nextphaserecruitment.com
Job Published: April 01, 2020 10:21

Job Description

Are you looking to lead global regulatory strategy for a pioneering Biopharmaceutical company?
 
My client is specialising in the development of vaccines and diagnostic kits for people who suffer from allergies. They have developed an innovative approach to medical treatments over a number of decades and are in an exciting phase of expansion across Europe and the USA. The company has an excellent reputation for its welcoming atmosphere, staff morale and ongoing career development. They have a range of ongoing clinical trials in different countries and have created this new position in order maximise their new product pipelines.
 
The Role

Your role will be to lead the global regulatory strategy and execution for the relevant product development, to ensure successful approvals and launches across the designated territories. You will be providing expert guidance and support to R&D and commercial teams to enhance the value of the company pipeline. Your role will encompass leading interactions with health authorities as well as developing & improving procedures for the broader regulatory strategy group.
 
Benefits

In addition to a competitive salary (negotiable depending on experience), the company offers a very good benefits package including:

  • Annual bonus (discretionary and non-contractual)
  • Appropriate expenses for international travel (accommodation and travel costs)
  • Stakeholder pension plan
  • Life insurance scheme
  • 25 days’ holiday
  • Long term disability scheme
  • Private medical plan

 

Experience
The successful candidate will have extensive regulatory experience in the biotech/pharma industry, with a broad knowledge and experience of drug development and approval requirements for Europe and/or US. Proven experience of leading & managing submissions and approvals, alongside a deep understanding of relevant legislation & international guidelines, is essential.

Full details will be provided on application.