Clinical Research Associate

Clinical Research Coordinator Location: Actalent Florence, Italy Metropolitan Area Actalent, a leading CRO, is looking for a Clinical Research Coordinator in Florence, Italy. This is an exciting opportunity to start as soon as possible and gain industry experience. The Clinical Research Coordinator must have a minimum of 2 years clinical research experience...

A leading CRO are looking for a Clinical Research Coordinator in Florence, Italy. This is an exciting opportunity with candidates to start as soon as possible and great opportunity to gain industry experience. The Clinical Research Coordinator must have minimum 2 year clinical research experience as the CRO need an individual who can work independently as...

A leading CRO are looking for a Clinical Research Coordinator in Florence, Italy.This is an exciting opportunity with candidates to start as soon as possible and great opportunity to gain industry experience.The Clinical Research Coordinator must have minimum 2 year clinical research experience as the CRO need an individual who can work independently as well...

A leading CRO are looking for a Clinical Research Coordinator in Florence, Italy.This is an exciting opportunity with candidates to start as soon as possible and great opportunity to gain industry experience.The Clinical Research Coordinator must have minimum 2 year clinical research experience as the CRO need an individual who can work independently as well...

OverviewPOSITION SUMMARY: The Senior Clinical Research Associate (Senior CRA) is responsible for scheduling and conducting on-site and remote monitoring visits in compliance with applicable regulatory standards (MDR, ISO *****, ICH/GCP guidelines, Teleflex procedures and IRB/EC policies and procedures).The Senior CRA conducts monitoring visits as identified...

Overview POSITION SUMMARY: The Senior Clinical Research Associate (Senior CRA) is responsible for scheduling and conducting on-site and remote monitoring visits in compliance with applicable regulatory standards (MDR, ISO 14155, ICH/GCP guidelines, Teleflex procedures and IRB/EC policies and procedures). The Senior CRA conducts monitoring visits as...

A leading medical device company in Tuscany is seeking a Senior Clinical Research Associate to conduct monitoring visits and ensure compliance with regulatory standards.The ideal candidate will have at least 5 years of clinical trial monitoring experience, strong communication skills, and the ability to work independently.Proficiency in both Italian and...

A leading medical device company in Tuscany is seeking a Senior Clinical Research Associate to conduct monitoring visits and ensure compliance with regulatory standards. The ideal candidate will have at least 5 years of clinical trial monitoring experience, strong communication skills, and the ability to work independently. Proficiency in both Italian and...

A global healthcare solutions company in Tuscany is looking for a Clinical Research Associate to manage and monitor clinical sites ensuring compliance with regulations.The ideal candidate will have a Master's degree, 2-3 years of independent monitoring experience, and proficiency in both Italian and English.This role offers a competitive salary and diverse...

A global healthcare solutions company in Tuscany is looking for a Clinical Research Associate to manage and monitor clinical sites ensuring compliance with regulations. The ideal candidate will have a Master's degree, 2-3 years of independent monitoring experience, and proficiency in both Italian and English. This role offers a competitive salary and diverse...