Legal Coordinator (m/v)

☞ MEDPACE BELGIUM

Aussicht: 130

Update Tag: 16-11-2025

Ort: Heverlee Flemish Brabant

Kategorie: Finanzen / Bank / Aktien

Industrie:

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Jobinhalt

Overview

Medpace is a scientifically-driven, global, full-service clinical contract research organization (CRO) providing Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Medpace¿s mission is to accelerate the global development of safe and effective medical therapeutics through its high-science and disciplined operating approach. We leverage local regulatory and deep therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, Medpace employs approximately 2,700 people across 36 countries.

Job Summary

Our clinical operations activities are growing rapidly, and we are currently seeking a full-time, office-based Contract Specialist to join our Clinical Operations team. This position plays a key role in the study start-up and clinical trial management processes at Medpace. The Site Contract Specialist will play a key role in advancing the start-up of our projects. If you want an exciting career where you use your previous expertise and can develop and grow your career even further, then this is the opportunity for you.

Responsibilities

  • Drafting, reviewing, negotiating, and finalizing agreements, termination letters or other legal documents required for a clinical study;
  • Negotiate within client approved contract and budget templates and negotiation parameters;
  • Identify and assesses legal, financial, and operational risksand escalate to appropriate Contract Lead or Contract Manager;
  • Provide recommendations and alternative resolutions throughout negotiations using established escalation channels;
  • Coordinate with internal functional departments to ensure various site startup activities are aligned with contractual process and mutually agreed up timelines; and
  • Keep up to date with applicable local regulations impacting clinical trial contracts.

Profil

Qualifications

  • Bachelor’s degree; preferable in Law or Sciences.
  • At least 1 year of relevant work experience;
  • Prior contract negotiation experience preferred but not required;
  • Strong attention to detail and excellent communication skills; and
  • Excellent knowledge of the English + Dutch or French language.

Travel:None

Connaissances linguistiques

Nederlands : Middelmatige
Engels : Middelmatige
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Frist: 31-12-2025

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