Lavori attuali relativi a Senior Clinical Research Monitor — On-Site - firenze - JR Italy


  • Firenze, Italia Jr Italy A tempo pieno

    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...


  • firenze, Italia JR Italy A tempo pieno

    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...


  • Firenze, Italia JR Italy A tempo pieno

    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 14155, ICH/GCP guidelines, Teleflex procedures and IRB/EC policies and procedures). The Senior CRA conducts monitoring visits as identified...


  • firenze, Italia JR Italy A tempo pieno

    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 14155, ICH/GCP guidelines, Teleflex procedures and IRB/EC policies and procedures). The Senior CRA conducts monitoring visits as identified...


  • Firenze, Italia Jr Italy A tempo pieno

    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...


  • Firenze, Italia Translational Oncology Research, LLC A tempo pieno

    If you are an experienced CRA who is passionate about oncology research and looking to join a highly skilled and knowledgeable team, TRIO is the place for you! Translational Research in Oncology (TRIO) is a global clinical research organization dedicated to advancing translational cancer research in the clinical trial setting. Our passionate team is...


  • Firenze, Italia Translational Research in Oncology A tempo pieno

    If you are an experienced CRA who is passionate about oncology research and looking to join a highly skilled and knowledgeable team, TRIO is the place for you! Translational Research in Oncology (TRIO) is a global clinical research organization dedicated to advancing translational cancer research in the clinical trial setting. Our passionate team is...


  • Firenze, Italia Translational Research in Oncology A tempo pieno

    A global clinical research organization is seeking an experienced Clinical Research Associate to join their Monitoring Resources team. The role involves conducting site visits, ensuring compliance with regulations, and mentoring junior staff. Candidates should have at least 2 years of oncology trial monitoring experience, be fluent in English, and hold a...


  • firenze, Italia Red Bull Gruppe A tempo pieno

    Our client is a leading company in the Pharma Sector.We are seeking a Senior Clinical Research Associate to join our teamYou new roleEnsure compliance with client SOPs, study protocols, ICH-GCP and applicable regulationsTrain and support investigator site teams on study procedures and systemsConduct site initiation, monitoring (on-site and remote), and...


  • firenze, Italia Baker Hughes A tempo pieno

    Our client is a leading company in the Pharma Sector.We are seeking a Senior Clinical Research Associate to join our teamYou new roleEnsure compliance with client SOPs, study protocols, ICH-GCP and applicable regulationsTrain and support investigator site teams on study procedures and systemsConduct site initiation, monitoring (on-site and remote), and...

Senior Clinical Research Monitor — On-Site

8 ore fa


firenze, Italia JR Italy A tempo pieno

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 English is required. This role involves significant travel (up to 70%) and includes training and supporting site staff.#J-18808-Ljbffr