M

Medpace

Global CRO delivering full-service clinical trials

Laboratory Project Coordinator

Clinical Research OperationsConfirmed live in the last 24 hours
Full-timeCincinnati, OH, USANo salary listed

About the Job

Requirements

  • A bachelor's degree in science or a health-related field is required.
  • Laboratory experience is preferred.
  • Excellent oral and written communication skills are required.

Responsibilities

  • Create and maintain general and study-specific laboratory manuals and other study-related documents.
  • Develop and present clinical laboratory presentations at investigator meetings.
  • Design specifications and monitor production of specimen collection kits.
  • Track study status as appropriate.
  • Communicate all aspects of the protocol to internal departments for appropriate study setup, maintenance, and closeout.
  • Write, establish, and revise relevant Standard Operating Procedures and work instructions.

Desired Qualifications

  • Laboratory experience.

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

Recently Posted Jobs

Explore more opportunities at Medpace

See more jobs