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Medpace

Global CRO delivering full-service clinical trials

Experienced Clinical Research Associate - Clinical Research Associate

Clinical Research OperationsConfirmed live in the last 24 hours
Full-timeRemote in Italy€43k - €76k /yr

About the Job

Requirements

  • A master's degree in a health-related field is required.
  • CRA certification must be completed as per DMC 15/11/2011.
  • Previous experience as a Clinical Research Associate is required.
  • Willingness to travel nationally up to 60–80% is required.
  • Familiarity with Microsoft Office is required.
  • Fluency in English and Italian is required.

Responsibilities

  • Conduct qualification, initiation, monitoring, and closeout visits at research sites in compliance with the approved protocol.
  • Communicate with medical site staff, including coordinators, clinical research physicians, and other site staff.
  • Verify adequate investigator qualifications, training, and resources, including facilities, laboratories, equipment, and staff.
  • Verify medical records and research source documentation against case report form data, inform site staff of entry errors, ensure good documentation practices are followed, and communicate protocol deviations according to standard operating procedures, Good Clinical Practice, and applicable regulatory requirements.
  • Verify that the investigator is enrolling only eligible subjects.
  • Review regulatory documents.
  • Account for and inventory medical devices and/or investigational products or drugs.
  • Verify and review adverse events, serious adverse events, concomitant medications, and corresponding illnesses to confirm accurate data reporting in accordance with the protocol.
  • Assess the clinical research site's patient recruitment and retention success and offer suggestions for improvement.
  • Complete monitoring reports and follow-up letters, including summaries of significant findings, deviations, deficiencies, and recommended actions to secure compliance.

Desired Qualifications

  • Strong communication and presentation skills are considered a plus.

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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