Clinical Team Lead - Utrecht

Vacancy information

Publication date:March 10 2021
Employment type: Permanent
Sector: Biotechnical
Function Group: Clinical Research

Function Group: Clinical Research / Clinical Management

Organization

An international Clinical Research Organisation which specialises in brain, heart and immunology diseases is looking for a Clinical Team Lead (CTL). You as a CTL will be provided with space to be creative in monitoring- & site management in multiple regions, providing guidance to CRA teams and different international studies. You will be working together with three other CTL’s with whom you will be exchanging knowledge on a regular basis and/or you will be working independently on different case studies. As this is originally an academically founded CRO it is very science driven, focussing on the quality of research rather than the quantity. The environment stimulates people to think outside the box, come with ideas and build together towards a continuously improving clinical research provider.

Function

The CTL is positioned as a cornerstone in clinical activities, managing the research, development, testing and delivery of both quality and quantity. You will monitor the clinical activities according to the different protocols, SOPs, legal bounds and ICH-GCP guidelines. The communication between sponsor, Project Manager and the CRA team is expected to be executed in a consistent and effective manner. Your involvement with the CRA team is broad and extensive consisting of study guidance, training, meetings, external inspections and audits. While you are active as a CTL, you will be engaged with the development of relevant documentation, collaborate with data management and properly deliver reporting of adverse events, serious adverse events and suspected unexpected serious adverse reactions. In case you are an experienced CRA ready to lead, let me know and I can set up introductions.

Requirements

To be successful as a CTL within this dynamic environment you will need to:

  • Preferably be educated in a (bio)medical field on at least a Bachelor level
  • Have spent three years as a CRA in pharmaceutics and/or in the CRO sector
  • Preferably have experience in managing CRAs
  • Have knowledge of relevant legal guidelines like ICH/GCP
  • Have experience with global studies, written and spoken in Dutch and English

Offer

To acknowledge you for your indispensable qualities, we like to offer you:

  • An environment that celebrates innovation in an open, inspiring and dynamic culture under proper working conditions
  • Creating impact on the workfloor is possible by operating in an environment that salutes creativity and celebrates initiatives
  • Working in a beautiful building that is not only logistically attractive but is just as inspiring as your co-workers
  • Proper secondary benefits and a base salary with a midpoint of around €65000.- gross per year

Application

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

Yvo Selderbeek
Senior Associate – Clinical Research

+31(0)6-12576648
+31(0)23-7548660
y.selderbeek@qtcrecruitment.com

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