Senior Clinical Research Associate - Monitoring (Italy)

JR Italy; Perugia; In loco; EUR 40.000 - 60.000; Tempo pieno

Descrizione del lavoro

A leading medical device company in Perugia is seeking a Senior Clinical Research Associate responsible for conducting monitoring visits and ensuring compliance with regulatory standards. The ideal candidate will have at least 5 years of experience in clinical trial monitoring, excellent attention to detail, and the ability to train site staff. The position offers a competitive salary and the opportunity for professional development in a dynamic environment.

Competenze

• A minimum of 5 years’ on-site monitoring research experience as a CRA in the medical device or pharmaceutical industry.
• Strong working knowledge of MDR, ISO 14155 and ICH/GCP guidelines.
• Ability to train and mentor Clinical Studies personnel.

Mansioni

• Conducts monitoring visits to ensure compliance with regulatory standards.
• Evaluates quality and integrity of site practices while escalating quality issues.
• Prepares Monitoring Visit Reports per Teleflex procedures.

Conoscenze

Clinical trial monitoring skills

High attention to detail

Excellent communication skills

Organizational ability

Formazione

Bachelor’s or higher-level degree in life sciences

Strumenti

MS Word and Excel

Descrizione del lavoro

A leading medical device company in Perugia is seeking a Senior Clinical Research Associate responsible for conducting monitoring visits and ensuring compliance with regulatory standards. The ideal candidate will have at least 5 years of experience in clinical trial monitoring, excellent attention to detail, and the ability to train site staff. The position offers a competitive salary and the opportunity for professional development in a dynamic environment.