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.
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