Experienced Clinical Research Associate, Multi Sponsor

Medpace; Town of Italy (NY); Hybrid; USD 70,000 - 90,000; Full time

Benefits offered by this job

Flexible work environment

Competitive compensation and benefits package

Competitive PTO packages

Structured career paths with opportunities for professional growth

Company-sponsored employee appreciation events

Employee health and wellness initiatives

Job summary

Medpace, Inc. is seeking full-time Clinical Research Associates to join their team in the United States. The role involves conducting visits at research sites, ensuring compliance with protocols, and communicating effectively with site staff. Candidates should hold a Master’s degree in a health-related field and CRA certification. The position requires fluency in English and Italian, along with a willingness to travel extensively. Medpace offers a flexible working environment and opportunities for professional growth.

Qualifications

• Experience as CRA required.
• Willingness to travel up to 60-80% nationally.

Responsibilities

• Conduct qualification, initiation, monitoring, and closeout visits.
• Communicate with medical site staff.
• Verify investigator qualifications and resources.
• Ensure compliance with documentation practices.

Skills

Fluent in English

Fluent in Italian

Strong communication and presentation skills

Familiarity with Microsoft Office

Education

Master degree in health-related field

CRA certification completed

Job description

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;
• Communication 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;
• Medical record and research source documentation verification against case report form data, including informing the site staff of any entry errors, ensuring good documentation practices are being adhered to and communicating protocol deviations appropriately per SOPs, GCP, and applicable regulatory requirements;
• Verification that the investigator is enrolling only eligible subjects;
• Regulatory document review;
• Medical device and/or investigational product/drug accountability and inventory;
• Verification and review of 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 offering suggestions for improvement; and
• Completion of monitoring reports and follow-up letters, which includes providing summaries of the significant findings, deviations, deficiencies, and recommended actions to secure compliance.

Qualifications

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

Medpace Perks

• Flexible work environment
• Competitive compensation and benefits package
• Competitive PTO packages
• Structured career paths with opportunities for professional growth
• Company-sponsored employee appreciation events
• Employee health and wellness initiatives