Experienced Clinical Research Associate (Cra)

Buscojobs; Puglia; Remoto; EUR 40.000 - 60.000; Tempo pieno

Descrizione del lavoro

A leading contract research organization in Italy is seeking full-time Clinical Research Associates. The role involves conducting research site visits, ensuring compliance, and communicating with site staff. Candidates should have a Master's degree in a health-related field and CRA certification. Fluent English and Italian is required, along with a willingness to travel up to 80%. Flexible work environment and career growth opportunities are offered.

Servizi

Flexible work environment

Competitive compensation and benefits package

Generous PTO packages

Structured career paths

Employee health and wellness initiatives

Competenze

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

Mansioni

• Conduct visits at research sites in compliance with the protocol.
• Communicate with medical site staff.
• Verify investigator qualifications and resources.
• Review regulatory documents and adverse events.
• Complete monitoring reports summarizing findings.

Conoscenze

Fluent in English

Fluent in Italian

Strong communication skills

Presentation skills

Formazione

Master's degree in a health-related field

CRA certification completed

Strumenti

Microsoft Office

Descrizione del lavoro

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 record and research source documentation 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;
• Verify that the investigator is enrolling 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 ensure 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, summarizing significant findings, deviations, deficiencies, and recommended actions to ensure compliance.

Qualifications

• Master's degree in a health-related field;
• CRA certification completed as per DMC 15 / 11 / 2011;
• Previous experience as a CRA;
• Willing to travel up to 60-80% nationally;
• Familiarity with Microsoft Office;
• 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). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical, and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through a scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral, and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40+ countries.

Why Medpace?

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

The work we’ve done over the past 30+ years has positively impacted the lives of countless patients and families facing various diseases. The work we do today will improve the lives of people living with illness and disease in the future.

Medpace Perks

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

Awards

• Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023, and 2024
• Consistently awarded CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility

What to Expect Next

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