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Medpace

Global CRO delivering full-service clinical trials

Entry-Level Contract Specialist

Contract ManagementConfirmed live in the last 24 hours
Full-timeLeuven, BelgiumNo salary listed

About the Job

Requirements

  • A bachelor's degree is required; a degree in Law or Business is preferred.
  • At least 1 year of relevant work experience is preferred but not required.
  • Prior contract negotiation experience is preferred but not required.
  • Ability to work within a team environment and independently.
  • Strong attention to detail.
  • Strong written and spoken Dutch and English communication skills.
  • French language ability is a plus.
  • Submit a CV in English.

Responsibilities

  • Draft, review, negotiate, and finalize Clinical Site Agreements or other site-specific legal agreements required for a clinical study.
  • Act as the first-line subject matter expert for the assigned country regarding Clinical Site Agreement strategy, timelines, expectations, and execution challenges.
  • Negotiate within client-approved contract and budget templates and negotiation parameters.
  • Build relationships with sites and external stakeholders to accelerate site contract negotiations.
  • Identify and assess legal, financial, and operational risks, and escalate them to the appropriate Contract Lead, Contract Manager, or other internal stakeholders.
  • Provide recommendations and alternative resolutions throughout negotiations using established escalation channels.
  • Coordinate with internal functional departments to align site start-up activities with the contractual process and mutually agreed timelines.
  • Keep up to date with applicable local regulations affecting clinical trial contracts.

Desired Qualifications

  • A degree in Law or Business.
  • At least 1 year of relevant work experience.
  • Prior contract negotiation experience.
  • French language ability.

About the Company

Medpace

Global CRO delivering full-service clinical trials

Medpace is a global Contract Research Organization that provides end-to-end clinical development services for pharmaceutical, biotechnology, and medical device companies. It manages Phase I–IV trials from study design and regulatory submissions to monitoring, data management, biostatistics, and final reporting, using a single integrated team. A key differentiator is its ownership of integrated laboratories—global central labs, a bioanalytical lab, and imaging/ECG core labs—ensuring streamlined workflows and consistent data. Its physician-led, scientifically driven approach and single-vendor model aim to reduce sponsor oversight and help bring therapies to market efficiently, with operations in over 40 countries.

Company size
5,001-10,000
Company stage
IPO
Headquarters
Cincinnati, OH
Founded
1992

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