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Medpace

Global CRO delivering full-service clinical trials

Contract Specialist

Contract ManagementConfirmed live in the last 24 hours
ContractCincinnati, OH, USANo salary listed

About the Job

Requirements

  • A bachelor's degree in a related field of study is required.
  • Strong time-management and communication skills are required.
  • The candidate must be organized and detail oriented.

Responsibilities

  • Distribute and finalize clinical trial contracts with principal investigators and clinical study sites.
  • Negotiate contractual terms and budget requests within approved parameters.
  • Maintain open communication with assigned clinical sites and internal project team members about negotiation progress and contract finalization.

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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