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Clinical Submission Specialist Brussels

Permanent / Brussels Belgium

up to

Clinical Start Up Specialist Office Based Brussels

Our client is a top 5 global CRO which has enjoyed a number of years of positive growth. Due to this growth our Client is looking to hire experienced Clinical Start Up Specialists who will be office based in Brussels, Belgium.

Skills

  • Primary contact with investigative sites during site start-up activities
  • Conduct and facilitate specific start-up activities
  • Site identification, feasibilities, SRP collection,
  • ICF customization and approval, EC submissions,
  • Preparation and negotiation of Contract

Experience

  • Working knowledge of ICH, FDA, IRB/IEC
  • Experienced in the EC submission process for 3-5 years in Belgium
  • Experience with contract negotiation in Belgium
  • Good organizational and time management skills
  • Fluent in French, Dutch and English

 

Keywords: Clinical Research, Submission Specialist. Contract negotiation, EC submission, CAsubmission, study start up, Phase I, Phase II, Brussels, Bruxelles, Phase III, Phase IV, Belgium, Lead CRA, CRO, Pharma, Biotech, Clinical Regulatory Affairs Specialist

If you have difficulty in applying, have any questions or you cannot find what you are looking for please contact us on 0044 (0) 207 421 0000 or email info@life-science.co.uk. We regard all communication and correspondence as confidential. Full job descriptions are available on request.

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About us

Resourcing Life Science is a specialist recruitment agency, providing career advice and employment opportunities within the Pharmaceutical, Biotechnology, Medical Devices and Clinical Research industries across the globe.

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info@life-science.co.uk

0044 (0) 207 421 0000

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