Lavoro Clinical study coordinator Provincia di Monza e della Brianza

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...

A clinical research company is seeking a detail-oriented Central Study Coordinator for a part-time position in Italy. The role involves supporting the planning and coordination of clinical studies, maintaining documentation, and ensuring compliance with regulatory standards. Candidates should have a Bachelor’s in Life Sciences and GCP knowledge, with preferred experience as a CRA or CTA. This...

Evidilya, the dedicated Contract Research Organization of Sprim Health Group operates as a full-service international expertise in successfully developing and managing observational, pre-clinical and clinical trials in the field of Food&Nutrition, Pharma and Medtech/Medical Devices industries with a strong technological and digital footprint, is looking for a Study Project Manager Main Tasks: -...

The Senior Data Manager reports to the Data Manager Project Coordinator, serve as primary point of contact to the study team for clinical data related matters and ensure clinical data are managed in compliance with applicable standards, regulatory guidelines and OPIS SOPs. Some of what you'll do: Ensure data is managed in compliance with applicable standards (e.g., CDISC), regulatory guidelines...

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...

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...

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...

Clinical Project Manager – Italy Location:Milan, Italy Department:Clinical Operations / Project Management Employment Type:Full-time / Permanent About the Role We are seeking an experienced and proactiveClinical Project Manager (CPM)to lead and oversee the execution of clinical trials across Italy. Based inMilan, this position is responsible for theoverall management and delivery of clinical...

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,...

We are looking for a Data Manager on behalf of an R&D Company based near Milan. The candidate will report to the Chief Scientific Officer and CEO of the Company. Main responsibilities : Ensure data management activities of assigned studies are planned and executed according to project timelines, maintaining high standards of data integrity and quality, while adhering to budget...

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...

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...

Evidilya, the dedicated Contract Research Organization of Sprim Health Group operates as a full-service international expertise in successfully developing and managing observational, pre-clinical and clinical trials in the field of Food&Nutrition, Pharma and Medtech/Medical Devices industries with a strong technological and digital footprint, is looking for a Study Project ManagerMain Tasks:...

Position: Central Study Coordinator Location: Remote, Italy Employment Type: Part-time – 24 hours per week (Contract) Industry: Clinical Research / Life Sciences About the Role We are seeking a detail-oriented and proactive Central Study Coordinator to support the planning, execution, and oversight of clinical research studies. This remote opportunity within Italy serves as a central operational...

CRA II – Remote (Italy) | €45,000–€52,000 + 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 niche treatments, blockbuster drugs,...

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...

CRA II – Remote (Italy) | €45,000–€52,000 + 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 niche treatments, blockbuster drugs,...

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...