Seuss +

Clinial Team Lead

Seuss +
29 Sep 2021
29 Oct 2021
Clinical Research
Full Time
Contract Type
Experience Level
Experienced (non-manager)
Title: Clinical Team Lead
Location: The Netherlands
Contract type: Perm or Contract

Are you a senior or lead CRA looking to take a step into an operational role?

We have an exceptional opportunity for a motivated and dynamic Clinical Team Lead based in either The U.K or The Netherlands to join a scientific and open-minded CRO.

Are you the perfect candidate?

If you enjoy coordinating, managing and monitoring multiple clinical sites while fostering and enhancing the education and training of various international CRA teams, this is the role for you.

Your Qualifications
  • A higher level of education, preferably in a (bio)medical field.
  • A minimum of 3 years experience as CRA in the pharmaceutical and/or CRO industry.
  • Experience in coaching and training of CRAs is a pre.
  • Experience with therapeutic area cardiovascular and/or CNS is a pre.
  • Up-to-date knowledge of legislation and regulations and ICH/GCP guidelines.
  • Experience with multi-centre, international studies.
  • Experience with regulatory / EC submissions/ start-up phase of clinical studies.
Do you enjoy
  • Project flexibility?
  • Planning, organizing and executing international clinical trials from initial set up to study closure?
  • Managing clinical activities in various assigned countries in accordance with previously defined performance indicators in terms of both quality and quantity and implementing actions as necessary?
  • Monitoring clinical activities in accordance with protocol, SOPs, applicable laws and ICH-GCP guidelines?
  • Ensuring that information is conveyed effectively between the sponsor, Project Manager and CRA teams?
  • Being the Sponsor contact?
  • Ensuring adherence of the CRA team to study timelines?
  • Reviewing and monitoring visit reports?
  • Performing accompanied site visits, we required?
  • Contributeing to the development of study-specific documentation?
  • Training CRAs with regard to protocol, Case Report Form (CRF) and study-specific procedures?
  • Participating in, and jointly organizing meetings for investigators and CRAs?
  • Ensuring the correct query process is followed in collaboration with Data Management?
  • Ensuring the correct reporting and follow-up of Adverse Events, Serious Adverse Events and Suspected Unexpected Serious Adverse Reactions?
  • Supporting the CRA team during inspections by healthcare authorities or audits?
  • Ensuring the reliable documentation and archiving of study documents, both at the study site and 'in-house'?

Are you ready to become part of their story?

Are you looking for an organization that encourages ideas, out of the box thinking and offers a safe place to grow?

You'll enjoy an open culture in an innovative and dynamic environment with inspiring colleagues and good working conditions.

A newly appointed CEO brings a fresh vision and an abundance of new approaches for this growing, well-connected CRO.

Are you looking to make an impact on medicine and patient lives?
Join this progressive and innovative organization rooted in science, providing end-to-end CRO services in specific therapeutic areas and sought-after SMO services.

Our recruitment process

We go beyond traditional recruitment; we work closely with you to ensure an unrivalled, personal candidate experience throughout our entire process.

Our relationship with this client allows us to fully support you through the recruitment process, providing you with all the role insight and knowledge you need for this 2-part interview process.

Our recruitment process is entirely confidential. Your details will never be shared without your prior consent.
If you would like to be considered for this position, please send in your English CV in WORD format to

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