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Medpace

Global CRO delivering full-service clinical trials

Clinical Research Coordinator to Clinical Research Associate

Clinical Research OperationsUpdated on Nov 14
Full-timeRemote in USANo salary listed

About the Job

Requirements

  • A minimum of a Bachelor's degree in a health- or science-related field is required.
  • At least 2 years of experience as a Clinical Research Coordinator at the site level is required.
  • Ability to travel 60–70% to locations nationwide is required.
  • A valid driver's license is required.
  • Strong communication and presentation skills, attention to detail, and efficient time management are required.

Responsibilities

  • Conduct qualification, initiation, monitoring, and closeout visits at research sites in compliance with the approved protocol.
  • Collaborate with research site staff, including coordinators, physicians, and pharmacists.
  • Verify medical records and research source documentation against case report form data; work with site staff to resolve issues; ensure good documentation practices; and communicate protocol deviations according to standard operating procedures, good clinical practice, and applicable regulatory requirements.
  • Verify and review adverse events, serious adverse events, and concomitant medications to confirm accurate data reporting in accordance with the protocol.
  • Perform investigational product inventory and reconciliation; review storage and security; and verify that investigational product has been dispensed and administered to patients according to the protocol.
  • Routinely review the Investigator Site File for accuracy, timeliness, and completeness, and reconcile its contents with the Trial Master File.
  • Assess the research site's patient recruitment and retention success and offer suggestions for improvement.
  • Complete monitoring reports and follow-up letters documenting significant findings, deviations, deficiencies, and recommended actions to ensure compliance.

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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