This job has expired

Regulatory Project Manager

Barrington James
Paris (Ville), Ile-de-France (FR)
Start date
20 Jan 2023
Closing date
19 Feb 2023

View more

Job Details

Hiring has opened up for an experienced Regulatory Affairs Project Manager!

Barrington James are partnered with a cutting edge gene therapy company with expertise in rare diseases. This position is a good fit for those who're truly passionate about scientific development.

The job

  • Provide support to the project managers involved in the regulatory aspect and the development of products
  • Provide answers according to the stage of development of the project
  • Prepare writing of the documents that are part of the files of applications for clinical trial authorisations
  • Participate in the preparation of regulatory files for clinical trial authorisations outside the EU (US)
  • Coordinate the preparation of regulatory files for scientific advice
  • Coordinate regulatory activities involving external partners


  • Life Science degree
  • Three years minimum experience in regulatory affairs for biological products
  • Experience with European regulations (FDA is a plus)
  • Able to work in the Paris area at least 2 days in office
  • Fluent in both French and English


We’re great at what we do. A collection of the worlds finest Life Science recruiters working for the worlds best Life Science consultancy.

Originally, a purely contingency and contract recruiter, focused in the UK, Barrington James is now a sophisticated, highly effective provider of human resources solutions up to full RPO, partnering the pharma, medical devices, and healthcare industries right across the globe.

Find Us
01293 776644
Victoria House
Consort Way

Get job alerts

Create a job alert and receive personalised job recommendations straight to your inbox.

Create alert