Clinical Research Associate: Study Monitor

3 settimane fa


desio, Italia OPIS s.r.l. A tempo pieno

A biotech-focused CRO in Italy is seeking a Clinical Research Associate (CRA) to coordinate and oversee clinical studies, ensuring compliance with protocols and regulations. The ideal candidate should have a degree in a scientific field and up to 12 months of experience as a CRA. Responsibilities include site monitoring, interaction with regulatory teams, and managing study materials. This role offers a competitive salary and professional growth opportunities within a supportive environment.#J-18808-Ljbffr



  • Desio, Italia Opis A tempo pieno

    Clinical Research Associate (CRA) is responsible for coordinating and overseeing the execution of clinical studies, mainly observational, and clinical investigations under the supervision by the ProjectManager: identify, select, initiate and close-out appropriate investigational sites for clinical studiesand clinical investigations. To monitor those sites to...


  • Desio, Italia OPIS A tempo pieno

    Clinical Research Associate (CRA) is responsible for coordinating and overseeing the execution ofclinical studies, mainly observational, and clinical investigations under the supervision by the ProjectManager: identify, select, initiate and close-out appropriate investigational sites for clinical studiesand clinical investigations. To monitor those sites to...


  • Desio, Italia OPIS A tempo pieno

    Clinical Research Associate (CRA) is responsible for coordinating and overseeing the execution ofclinical studies, mainly observational, and clinical investigations under the supervision by the ProjectManager: identify, select, initiate and close-out appropriate investigational sites for clinical studiesand clinical investigations. To monitor those sites to...


  • desio, Italia OPIS s.r.l. A tempo pieno

    Clinical Research Associate (CRA) is responsible for coordinating and overseeing the execution of clinical studies, mainly observational, and clinical investigations under the supervision by the Project Manager: identify, select, initiate and close-out appropriate investigational sites for clinical studies and clinical investigations. To monitor those sites...


  • Desio, Italia OPIS A tempo pieno

    Clinical Research Associate (CRA) is responsible for coordinating and overseeing the execution of clinical studies, mainly observational, and clinical investigations under the supervision by the Project Manager: identify, select, initiate and close-out appropriate investigational sites for clinical studies and clinical investigations. To monitor those sites...


  • Desio, Italia OPIS A tempo pieno

    Clinical Research Associate (CRA) is responsible for coordinating and overseeing the execution of clinical studies, mainly observational, and clinical investigations under the supervision by the Project Manager: identify, select, initiate and close-out appropriate investigational sites for clinical studies and clinical investigations. To monitor those...


  • Desio, Italia OPIS A tempo pieno

    Clinical Research Associate (CRA) is responsible for coordinating and overseeing the execution of clinical studies, mainly observational, and clinical investigations under the supervision by the Project Manager: identify, select, initiate and close-out appropriate investigational sites for clinical studies and clinical investigations. To monitor those sites...


  • Desio, Italia OPIS A tempo pieno

    Clinical Research Associate (CRA) is responsible for coordinating and overseeing the execution of clinical studies, mainly observational, and clinical investigations under the supervision by the Project Manager: identify, select, initiate and close-out appropriate investigational sites for clinical studies and clinical investigations. To monitor those sites...


  • Desio, Italia OPIS s.r.l. A tempo pieno

    Clinical Research Associate (CRA) is responsible for coordinating and overseeing the execution of clinical studies, mainly observational, and clinical investigations under the supervision by the Project Manager: identify, select, initiate and close-out appropriate investigational sites for clinical studies and clinical investigations. To monitor those sites...


  • desio, Italia OPIS s.r.l. A tempo pieno

    Clinical Research Associate (CRA) is responsible for coordinating and overseeing the execution of clinical studies, mainly observational, and clinical investigations under the supervision by the Project Manager: identify, select, initiate and close-out appropriate investigational sites for clinical studies and clinical investigations. To monitor those sites...