Job Summary
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 use your previous expertise and can develop and grow your career even further, then this is the opportunity for you.
Medpace will provide comprehensive initial and ongoing training depending on your previous experience.
Responsibilities
* Conduct qualification, initiation, monitoring, and closeout visits at research sites in compliance with the approved protocol;
* Communicate with the medical site staff including coordinators, clinical research physicians, and their 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, 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 for accurate data reporting;
* Assess site’s patient recruitment and retention, and suggest improvements;
* Complete monitoring reports and follow-up letters, summarizing findings, deviations, deficiencies, and recommended actions.
Qualifications
* Master's degree in a health-related field;
* CRA certification as per DMC 15/11/2011;
* Previous experience as a CRA;
* Willingness to travel up to 60-80% nationally;
* Proficiency with Microsoft Office;
* Fluency 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 biotech, pharmaceutical, and medical device industries. Our mission is to accelerate the development of safe and effective therapeutics through scientific and disciplined approaches. Headquartered in Cincinnati, Ohio, with over 5,000 employees across 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 worldwide. The work we do today will improve future lives.
Medpace Perks
* Flexible work environment
* Competitive compensation and benefits
* Generous PTO packages
* Structured career growth opportunities
* Company-sponsored events
* Health and wellness initiatives
Awards
* Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021-2024
* Consistent CRO Leadership Awards from Life Science Leader magazine
What to Expect Next
A Medpace team member will review your qualifications and contact you for next steps if interested.
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