Vacancies

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

Kontich

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

Diegem

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

Gent

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

Brussels

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

North of Brussels

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

South of Antwerp

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.

South of Antwerp

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

Gent

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

Kontich

Tim
Janssen
Managing Partner

Do you want to learn more about Fern Valley? Are you interested in seeing how we can help your company grow? Let's get acquainted. I'll be delighted to hear your story and to share our vision. Experience the personal & open approach of Fern Valley and embark on a journey with us.

+32 487 10 61 46
tim.janssen@fern-valley.com