Position: Mid-Senior level

Job type: Full-time

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Looking for a new challenge?I am working with a top consultancy organization who are going from strength to strength. They work with some of the biggest names in pharmaceuticals and are renowned for their efficient market and product development.This company are looking for a heavily organised Specialist Early Access Management to join their regulatory function.Responsibilities
  • Quality data control management
  • Effectively manage and maintain professional relationships with clients and external stakeholders
  • Management of all patient inclusions including the organization of correct documentation
  • Support for AAP/AAC related activities
Essential Requirements
  • An effective project manager (in pharma, food manufacturing, chemical manufacturing, med devices)
  • Desired but not essential, experience in either the medical field or a CRO environment
  • Fluent in French and high-level standard of English
  • Seamless communicator with excellent organisation skills
If you are interested in working with a company that offers excellent career progression opportunities, then send your CV and application over to me today!Why wait?Email: egilbride@barringtonjames.com
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Deadline: 27-12-2025

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