Vacancy Clinical Team Lead – Zeist


Organization

29 AUG ’22: For a young and strongly growing organisation in the Clinical trial field we are looking for an ambitious Clinical Team Lead. The organisation distinguishes itself in combining the latest scientific insights with operational excellence to develop innovative solutions, enabling clients to bring their treatments to the market faster.

Function

As a Clinical Team Lead, you will be coordinating the Clinical Research Associates while maintaining the oversight position of site management. Moreover, this position is very much interesting as the collaboration with the Project Manager is intensive. This with the intention, if your ambitions align, to construct a professional development plan to become Project Manager within two years. During this process you will gradually be introduced to the different aspects of a Project Manager role. Herewith, you will be in direct communication with the sponsor regarding developments of the trial. You will join the Project Manager to design and write the project plan, which will introduce you to the common processes.

Moreover, you will act as a point of contact for the team on a tactical and strategic level, as well as for potential other CTLs assigned to the project. You are involved in one or more (international) studies as a singular CTL, or in larger studies, as part of a team of CTLs. Your work involves managing clinical activities in assigned countries in accordance with previously defined performance indicators focussed on quality. operationally, you will ensure that information and results are conveyed effectively between the sponsor, Project Manager and the CRA team. Finally, you will be focussed on the development of the CRAs by means of training with regard to protocol, CFR and study-specific procedures.

Requirements

You fit in this role perfectly if you have;

  • Higher level education (preferably (bio)medical focussed)
  • Current knowledge of legislation, regulations and IHC-GCP guidelines
  • At least 3 years experience as CRA within CRO’s or pharmaceutical industry
  • Experience with multi-centre international studies
  • Experience with regulatory, EC submissions and start-up phase of clinical studies
  • Strong command of the English language (Dutch is a pre)

Offer

If you enjoy flexibility and have a certain level of aspiration, and you want to have an impact, this organisation might be the perfect fit for you. Besides, the organisation offers:

  • A competitive base salary
  • ABP pension (70% employer / 30% employee)
  • 8% bonus arrangement
  • 30 holidays
  • Daily home work allowance
  • Travel allowance
  • Work-from-home budget of EUR 600

Application

If you are interested in this job, or in similar ones, please feel free to contact me directly.

Sander Westerhout
Associate | Biotechnology

+31 6 51 66 69 96
+31 23 754 86 60
s.westerhout@qtcrecruitment.com