- Conduct site qualification, initiation, monitoring, and closeout visits.
- Ensure compliance with study protocols, GCP, and regulatory requirements.
- Perform source data verification and data collection.
- Coordinate with study sites and investigators to ensure timely and accurate data submission.
- Contribute to site training and adherence to study procedures and protocols.
- Assist in the preparation and review of study documents and reports.
- Bachelor's degree in a health-related field or equivalent.
- Minimum of 2 years of experience as a CRA.
- Strong knowledge of GCP, ICH guidelines, and regulatory requirements.
- Excellent communication and organizational skills.
- Ability to work independently and as part of a team.
- Flexibility to travel to study sites within Italy.
- Annual Bonus
- Company car/ car allowance
- Fantastic work-life balance
- Competitive salary
- Wellness benefits
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Clinical Research Associate - Firenze, Italia - AL Solutions
Descrizione
Jordan Griffiths has partnered with a growing CRO who are looking for a dedicated Clinical Research Associate (CRA) to join their team in Florence. This is a fantastic opportunity to work on a variety of clinical trials across different therapeutic areas and contribute to advancing medical research.
Key Responsibilities:
Requirements
Requirements:
Benefits