Clinical Trial Manager — Flexible & Equity (Belgium)

Medpace, Inc.

Heverlee

Hybride

EUR 85 000 - 125 000

Plein temps

14 jours+
Générateur de candidature

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Avantages offerts par ce poste

Competitive compensation
Health and retirement benefits
WFH after training
Company-sponsored social events

Résumé du poste

Medpace is seeking an experienced Clinical Trial Manager to join our Belgium-based team in Leuven. You will oversee day-to-day project operations across Phases 1-4, act as primary Sponsor contact, and ensure compliance with ICH/GCP and contractual requirements.

We welcome experts in Oncology/Cardiovascular/Endocrine/Metabolic who can either continue in their area or expand to new therapeutic areas; remote flexibility is available for candidates with relevant experience.

Qualifications

  • Bachelor’s degree in health or life or life sciences; advanced degree preferred.
  • 3+ years of Clinical Trial Management experience, CRO experience preferred.
  • Experience in Phases 1-4; Phases 2-3 preferred.
  • Strong leadership skills; ability to manage timelines; bid defense experience preferred.

Responsabilités

  • Manage day-to-day operations of the project per contract and ICH/GCP requirements.
  • Serve as primary Sponsor contact for operational issues and study deliverables.
  • Maintain knowledge of protocol, therapeutic area, and indication.
  • Provide cross-functional oversight and ensure necessary training.
  • Review study protocol, edit checks, data analysis plan, and final report when applicable.
  • Develop operational project plans and manage risk; oversee vendors.
  • Manage site quality and supervise project CRAs and monitoring deliverables.

Connaissances

Trial management
Leadership
Bid defense
Phases 1-4 experience

Formation

Bachelor’s degree in health or life sciences
Advanced degree in health or life sciences

Description du poste

Medpace is seeking an experienced Clinical Trial Manager to join our Belgium-based team in Leuven. You will oversee day-to-day project operations across Phases 1-4, act as primary Sponsor contact, and ensure compliance with ICH/GCP and contractual requirements.

We welcome experts in Oncology/Cardiovascular/Endocrine/Metabolic who can either continue in their area or expand to new therapeutic areas; remote flexibility is available for candidates with relevant experience.

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