Regulatory Project Manager

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

Requirements

• 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