Experienced Clinical Research Associate (CRA)

Medpace; Italia; In loco; EUR 35.000 - 50.000; Tempo pieno

Descrizione del lavoro

A leading clinical research organization is seeking full-time Clinical Research Associates in Italy. This role involves site monitoring, compliance checks, and collaboration with medical staff. Ideal candidates will have a Master's degree and CRA certification, along with strong communication skills. Join a company committed to improving lives through clinical research.

Servizi

Flexible work environment

Competitive compensation and benefits

Generous PTO packages

Structured career development opportunities

Company-sponsored employee events

Health and wellness initiatives

Competenze

• Previous CRA experience required.
• Willing to travel 60-80% nationally.

Mansioni

• Conduct visits at research sites in compliance with protocols.
• Manage medical device and investigational product accountability.
• Complete monitoring reports summarizing findings.

Conoscenze

Communication

Presentation

Fluency in English

Fluency in Italian

Formazione

Master's degree in a health-related field

Strumenti

Microsoft Office

Descrizione del lavoro

Our clinical activities are growing rapidly, and we are currently seeking full-time, home or office-based Clinical Research Associates to join our Clinical Monitoring team in Italy. This position will work with a team to accomplish tasks and projects that are instrumental to the company’s success. If you want an exciting career where you can utilize your previous expertise and further develop your career, then this is the opportunity for you.

Medpace will provide comprehensive initial and ongoing training based on your previous experience.

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 their staff;
• Verify investigator qualifications, training, resources, 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, and communicate protocol deviations per SOPs, GCP, and regulatory requirements;
• Ensure investigator enrolls only eligible subjects;
• Review regulatory documents;
• Manage medical device and investigational product/drug accountability and inventory;
• Review adverse events, serious adverse events, concomitant medications, and illnesses to confirm accurate data reporting;
• Assess site’s patient recruitment and retention, offering suggestions for improvement;
• Complete monitoring reports and follow-up letters, summarizing findings, deviations, deficiencies, and recommended actions.

Qualifications

• Master's degree in a health-related field;
• Willing to travel 60-80% nationally;
• Familiarity with Microsoft Office;
• CRA certification as per DMC 15/11/2011;
• Previous CRA experience;
• Fluent in English and Italian;
• Strong communication and presentation skills are a plus.

Medpace Overview

Medpace is a full-service clinical contract research organization (CRO) providing Phase I-IV clinical development services to the biotech, pharmaceutical, and medical device industries. Our mission is to accelerate the development of safe and effective therapeutics through a scientific and disciplined approach. Headquartered in Cincinnati, Ohio, with over 5,000 employees across more than 40 countries.

Why Medpace?

People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today.

Our work over the past 30+ years has positively impacted countless patients and families facing various diseases. The work we do today will improve lives in the future.

Medpace Perks

• Flexible work environment
• Competitive compensation and benefits
• Generous PTO packages
• Structured career development opportunities
• Company-sponsored employee events
• Health and wellness initiatives

Awards

• Recognized by Forbes as one of America's Most Successful Midsize Companies (2021-2024)
• Recipient of CRO Leadership Awards from Life Science Leader magazine for expertise, quality, reliability, and compatibility

What to Expect Next

A Medpace team member will review your qualifications and contact you if interested with next steps.

EO/AA Employer M/F/Disability/Vets