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Medpace

Global CRO delivering full-service clinical trials

Clinical Trial Contract Specialist

Contract ManagementConfirmed live in the last 24 hours
Full-timeWarsaw, PolandNo salary listed

About the Job

Requirements

  • A bachelor's degree is required; a degree in Law or Life Sciences is preferred.
  • At least 2 years of relevant work experience is required.
  • Strong attention to detail is required.
  • Fluency in English and Polish is required.
  • Prior contract negotiation experience is preferred but not required.

Responsibilities

  • Draft, review, negotiate, and finalize agreements, termination letters, and other legal documents required for a clinical study.
  • Negotiate within client-approved contract and budget templates and negotiation parameters.
  • Identify and assess legal, financial, and operational risks and escalate them to the appropriate Contract Lead or Contract Manager.
  • Provide recommendations and alternative resolutions throughout negotiations using established escalation channels.
  • Coordinate with internal functional departments to ensure site startup activities align 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 Life Sciences is preferred.
  • Prior contract negotiation experience is preferred but not required.

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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