Lavoro Research associate Provincia di Monza e della Brianza

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 to ensure that studies are carried...

Senior Clinical Research Associate (Oncology) Working embedded with a leading global oncology-focused biopharmaceutical company We are partnering with a top-tier global biopharmaceutical organisation to support a growing oncology portfolio and are seeking an experienced Clinical Research Associate to join the team in an advanced, hands-on clinical role. This position offers the opportunity to...

Social network you want to login/join with: Senior Clinical Research Associate, monza col-narrow-left Client: Teleflex Location: Job Category: Other - EU work permit required: Yes col-narrow-right Job Reference: 8556790222002585600337119 Job Views: 2 Posted: 27.08.2025 Expiry Date: 11.10.2025 col-wide Job Description: POSITION SUMMARY: The Senior Clinical Research Associate...

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...

Senior Clinical Research Associate – Remote (Italy) | €50,000 - €65,000 + Car Allowance Ready to take the next step in your CRA career? This is your chance to join a leading global organization that prioritizes your development and success. You’ll work remotely with approximately 6–8 site visits per month across Italy, gaining exposure to diverse protocols and therapeutic areas - including...

Pivotal is excited to expand our team and we are looking for an experienced, highly motivated Clinical Research Associate who shares our vision of providing clinical research excellence. Joining Pivotal as a CRA/SCRA means that you’ll enjoy being a member of one of the leading full-service contract research organizations in Europe with a very solid reputation. This role promises to gain direct...

Company Description Phidealive, established in ****, is a Contract Research Organization (CRO) with a strong foundation in Italy's rich clinical research culture. Positioned as a Clinical Research Atelier, Phidealive emphasizes scientific rigor, regulatory compliance, and a tailored operational approach for each project. The company collaborates with Pharma, Biotech, Medical Device, Food...

Your new company Our client is a leading company in the Pharma Sector. We are seeking a Senior Clinical Research Associate to join our team You new role Ensure compliance with client SOPs, study protocols, ICH-GCP and applicable regulations Train and support investigator site teams on study procedures and systems Conduct site initiation, monitoring (on-site and remote), and close-out...

ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development. The Field CRA is responsible for monitoring and management of clinical sites. This position focuses on all activities required to evaluate,...

Veeda Lifesciences is seeking a Clinical Research Associate (CRA) based in Italy for its growing international hematology/oncology Clinical Trials program. This is a full-time job. Job overview: The CRA is responsible for ensuring that the conduct of a clinical trial at selected Investigational Sites is according to the currently approved protocol/amendments, ICH GCP guidelines, the applicable...

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 *****, ICH/GCP guidelines, Teleflex procedures and IRB/EC policies and procedures). The Senior CRA conducts monitoring visits as identified by the monitoring plan, study team or...

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...

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 accuracy. Competitive salary and...

Pivotal is excited to expand our team and we are looking for an experienced, highly motivated Clinical Research Associate who shares our vision of providing clinical research excellence. Joining Pivotal as a CRA/SCRA means that you’ll enjoy being a member of one of the leading full-service contract research organizations in Europe with a very solid reputation. This role promises to gain direct...

A leading medical device company in Monza seeks a Senior Clinical Research Associate to ensure compliance during monitoring visits and maintain data integrity. Candidates should have a minimum of 5 years of experience in clinical trials, a degree in life sciences, and strong knowledge of MDR and ICH/GCP guidelines. This role requires excellent organizational and interpersonal skills, along with...

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 to ensure that studies are carried...

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 ensure that studies are carried out...

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 to ensure that studies are carried out...

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 to ensure that studies are carried out...

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 accuracy. Competitive salary and...