Clinical Research Associate: Study Monitor

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,...

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,...

Clinical Research Associate (CRA) 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...

A leading biotech CRO in Italy is seeking a Clinical Research Associate (CRA) to coordinate clinical studies and ensure compliance with protocols. The ideal candidate will possess a degree in a scientific field, preferably with some experience in clinical research. Responsibilities include conducting feasibility studies, monitoring sites, and ensuring data...

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...

Clinical Research Associate (CRA)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...

Clinical Research Associate (CRA)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...

Clinical Research Associate (CRA) 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...

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...

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...