Clinical Research Associate II
Descrizione dell'offerta
CRA II
Location: Milan (Hybrid)
THIS ROLE REQUIRES A MINIMUM OF 2 DAYS PER WEEK IN THEIR OFFICES IN MILAN
About the Company
The company is a well-established CRO, dedicated to maintaining the highest quality standards in the industry while conducting clinical studies across various therapeutic indications.
About the Role
As a Clinical Research Associate, you will enjoy a variety of monitoring tasks and work on clinical studies in different therapeutic indications, maintaining the highest quality standards in the industry.
Responsibilities:
- Conduct and report all types of onsite monitoring visits (5-6 days on site, per month)
- Perform study startup activities
- CRF review, source document verification
- Site Communication / Site Management
- Prepare for, participate in audits and inspections.
- Keep project teams informed of progress, issues, and timelines.
Required Experience:
- Degree in Life Sciences or similar (or equivalent experience/education)
- At least 2 years of independent on‐site monitoring in Italy; experience in Phase II & III trials.
- Therapeutic area experience (e.g., Oncology / Gastroenterology) is a strong plus
- Full working proficiency in English and Italian
Please reach out to Chris Boateng at