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Medpace

Global CRO delivering full-service clinical trials

Associate Director - Clinical Trial Management

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

About the Job

Requirements

  • A bachelor's degree in a health-related field is required.
  • At least 5 years of experience as a project or clinical trial manager within a contract research organization is required.
  • Experience in Phases 1–4 is required.
  • Experience managing the overall project timeline is required.
  • Strong leadership skills are required.

Responsibilities

  • Manage and provide accountability for day-to-day project operations according to the contract, ICH/GCP, and 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 project-specific training is provided.
  • Review and provide input for 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, where applicable.
  • Manage site quality and monitoring deliverables.

Desired Qualifications

  • An advanced degree in a health-related field is preferred.
  • Experience in Phases 2–3 is preferred.
  • Bid defense experience 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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