Clinical Trial Manager — Flexible & Equity (Belgium)

Medpace, Inc.

Heverlee

Hybrid

EUR 85.000 - 125.000

Vollzeit

14 Tage+

Eine vollständige Bewerbung in einer Minute

Maßgeschneiderter Lebenslauf und Anschreiben – versandbereit.

Schaffe es an den ATS-Filtern vorbei

Benefits dieser Stelle

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

Zusammenfassung

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.

Qualifikationen

  • 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.

Aufgaben

  • 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.

Kenntnisse

Trial management
Leadership
Bid defense
Phases 1-4 experience

Ausbildung

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

Jobbeschreibung

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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