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Medpace

Global CRO delivering full-service clinical trials

Director Study Start-Up Project Management

Clinical Research OperationsConfirmed live in the last 24 hours
Full-time

About the Job

Requirements

  • Study start-up and regulatory submissions experience within a contract research organization is required.
  • A bachelor's degree in Life Sciences or a related field is required.
  • At least 8 years of experience as a study start-up senior leader within a contract research organization is required.
  • Excellent presentation, negotiation, documentation, leadership, team-orientation, and interpersonal skills are required.
  • Strong customer focus and the ability to manage challenging priorities and remain flexible and adaptive in stressful situations are required.
  • Excellent written and oral communication skills are required.
  • Experience managing and developing a team is required.

Responsibilities

  • Contribute directly to the growth and strategic development of a large, global Study Start-Up team.
  • Develop and identify continuous improvement opportunities for internal processes.
  • Oversee Study Start-Up/Regulatory Submissions activities and timelines to ensure they comply with Medpace standard operating procedures and study protocols.
  • Provide input on new business development opportunities.
  • Develop and maintain relationships with clients.

Desired Qualifications

  • An advanced degree 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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