CRA

EPM Scientific is currently partnering with a l company that is seeking a Clinical Research Associate (CRA) with experience in cardiology. This is a part-time (approximately 0.3 FTE) contract position based in Italy, with a duration of 16 months.

The CRA will support the execution of clinical trials, ensuring compliance with regulatory standards and study protocols. This is an excellent opportunity for professionals seeking a flexible role in a collaborative and innovative environment.

Key Responsibilities:

• Conduct site selection, initiation, monitoring, and close-out visits
• Ensure compliance with GCP, study protocols, and regulatory requirements
• Perform source data verification and ensure data accuracy
• Maintain study documentation and timely reporting
• Facilitate communication between study sites and the sponsor
• Support patient safety and data integrity throughout the trial

Candidate Requirements:

• Prior experience as a CRA, ideally in medical device trials
• Background in cardiology or cardiovascular studies preferred
• Strong knowledge of GCP and EU clinical trial regulations
• Excellent organizational and communication skills
• Ability to work independently and manage multiple sites
• Fluency in English; Italian language skills are a plus

Details:

Location: Italy
Contract: Part-time (0.3 FTE) / 16 months
Therapeutic Area: Cardiology
Sector: Medical Devices

To learn more, please get in touch.