Head of Clinical Trials

Head of Clinical Trials

Centogene

Rostock, Germany

Your tasks will be:

  • Management and execution of international, multicenter clinical studies, including study protocol preparation, ethics approval applications, contract and ID preparation;
  • Leads all occurring activities of clinical study projects to ensure compliance with protocols, clinical objectives and regulatory requirements;
  • Acquisition of international, clinical trial centers;
  • Direct contact with recruiting centers and involved physicians;
  • Direct communication with clinical study centers for legal, study protocol, ethics approval, logistics topics;
  • Study center visits (e.g., initiation and close-out visits);
  • Analyzes clinical trial data to identify, develop and affect changes required for improvement and compliance;
  • Attend scientific meetings and conferences;
  • Support development of study designs, reports and protocols;
  • Maintains legal and regulatory requirements;
  • Plans and executes clinical trial projects.

You have the following skills and qualifications:

  • Thorough track record in health care/life sciences;
  • Good experience in managing clinical trials;
  • Solid expertise in working within regulatory and legal frameworks;
  • Distinctive communication and organization skills;
  • Fluent written and verbal English skills;
  • Well-experienced in team leading.

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© EuroJobsites 2020

EuroJobsites is a registered company number: 4694396 VAT number: GB 880 9055 04

Registered address: EuroJobsites Ltd, Unit 8, Kingsmill Business Park, Kingston Upon Thames, London, KT1 3GZ, United Kingdom

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