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Medpace

Global CRO delivering full-service clinical trials

Executive Director - Clinical Trial Project Management

Clinical Research OperationsConfirmed live in the last 24 hours
Full-timeCincinnati, OH, USAIn-person

About the Job

Requirements

  • A bachelor's degree in life sciences or a medical field is required; a master's or PhD in one of these fields is preferred.
  • Experience successfully leading international contract research organization project management or clinical trial management teams is required.
  • Proven ability to lead and motivate staff, think strategically, and execute organizational strategy is required.

Responsibilities

  • Manage and provide accountability for day-to-day project operations as defined by the contract and in accordance with ICH/GCP and all applicable laws, rules, and regulations.
  • Serve as the primary sponsor contact for operational project-specific issues and study deliverables.
  • Maintain in-depth knowledge of the protocol, therapeutic area, and indication.
  • Provide cross-functional oversight of internal project team members and deliverables, including ensuring all necessary project-specific training is provided.
  • Review and provide input on the study protocol, edit check specifications, data analysis plan, and final study report, when applicable.
  • Develop operational project plans.
  • Manage risk assessment and execution.
  • Manage study vendors.
  • Manage site quality, including directly supervising project Clinical Research Associates and monitoring deliverables.

Desired Qualifications

  • A master's or PhD in life sciences or a medical field is preferred.

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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