Upsilon Global are seeking two experienced Freelance Senior Clinical Research Associates to support an upcoming Cardiology Medical Device Study in Italy.
Indication: Cardiology (Medical Devices)
Medical Device Class: II and III
Study Duration: 6–12 months (depending on trial progression)
FTE: 0.5
Key Responsibilities:
Monitor clinical study sites in the cardiology therapeutic area, ensuring compliance with study protocols, regulatory requirements, and ICH-GCP standards.
Conduct site visits across all trial phases, from study initiation to close-out visits.
Ensure data accuracy, integrity, and patient safety throughout the study.
Collaborate effectively with clinical sites, vendors, and project teams to ensure smooth study progression.
Study Requirements:
10+ years of experience as a Senior CRA, with a strong background in cardiology and/or medical device studies.
Extensive knowledge of Italian regulatory requirements and compliance standards.
Ability to work independently while maintaining strong collaboration with site teams and sponsors.
Flexibility and willingness to travel to clinical sites across Italy as required.
Please apply via the advert or contact Juliana Madiba to discuss the opportunity.
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