Je bent verantwoordelijk voor de voorbereiding, coördinatie en opvolging van de klinische studies.

The Regulatory Affairs Officer reports to the Associate Director, Regulatory Affairs Strategy and interacts with the Global Strategic Implementation team, Regulatory Affairs counterparts cross fran

For the expansion of our client's clinical team, we are looking for a Clinical Data Manager (CDM).

We are responsible for all clinical supplies of the Research & Development portfolio and the Global Medical Affairs portfolio.

The main function of a clinical research associate (CRA) is to monitor clinical trials and ensure that clinical trials adhere to established guidelines, regulations and Standard Operating Procedure

As a TMF Specialist, you will be the Trial Master File (TMF) Subject Matter Expert and advisor for the Clinical Study Assistants (CSA), and other TMF stakeholders to ensure a complete and accurate

As a TMF Owner, you will be TMF Subject Matter Expert and advisor for the Clinical Study Teams on (e)TMF set-up, management, close-out and quality control to ensure a complete and accurate TMF.

For the expansion of our Regulatory Affairs team, our customer is looking for a Regulatory Affairs Manager to support the teams in preparation of Regulatory submissions including CTAs/briefing docu

Je bent verantwoordelijk voor de voorbereiding, coördinatie en opvolging van de klinische studies.

Being a CRA at Fern Valley means becoming part of a group of high quality specialists.