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Medpace

Global CRO delivering full-service clinical trials

Study Start-Up Project Manager

Clinical Research OperationsConfirmed live in the last 24 hours
Full-timeDallas, TX, USA

About the Job

Requirements

  • A bachelor's degree is required.
  • At least 5 years of experience in clinical research is required; experience at a contract research organization in Study Start-Up or as a Research Manager at a study site is preferred.
  • Project management experience and a demonstrated role in developing others are required.
  • Strong oral and written communication skills are required.

Responsibilities

  • Manage the successful execution of clinical trial start-up, maintenance, and close-out.
  • Lead others in a matrix environment.
  • Perform quality checks on submission documents and site essential documents.
  • Prepare and approve informed consent forms.
  • Serve as the Sponsor point of contact for start-up and regulatory submission items.
  • Review pertinent regulations to develop proactive solutions to start-up challenges.
  • Prepare new business proposals and present during bid defenses, general capabilities meetings, and audits.
  • Contribute to the growth and development of departmental staff, processes, and systems.

Desired Qualifications

  • An advanced degree in Life Sciences is preferred.
  • Experience at a contract research organization in Study Start-Up or as a Research Manager at a study site 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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