Clinical Trial Manager

Clinical Trial Manager

Medpace

Rotterdam, Netherlands

Responsibilities

  • Manage and provide accountability for day-to-day operations of the project, as defined by the contract and according to ICH/GCP and all other applicable laws, rules, and regulations;
  • Serve as primary Sponsor contact for operational project-specific issues and study deliverables;
  • Maintain in depth knowledge of protocol, therapeutic area, and indication;
  • Provide cross-functional oversight of internal project team members and deliverables, which includes ensuring all necessary project-specific training is provided;
  • Review and provide input for study protocol, edit check specifications, data analysis plan, and final study report, when applicable;
  • Develop operational project plans;
  • Manage risk assessment and execution;
  • Responsible for management of study vendor;
  • Manage site quality, including direct supervision of project Clinical Research Associates and monitoring deliverables.

Qualifications

  • Mimimum Bachelor’s degree in a health related field; Advanced degree in a health related field preferred;
  • Experience in Phases 1-4; Phases 2-3 preferred;
  • Bid defense experience, preferred;
  • 3-5 years in project management/clinical trial management in clinical research industry;
  • Strong leadership skills.

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© EuroJobsites 2022

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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