Clinical Site Manager 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. You'll utilise your extensive therapeutic knowledge in Oncology to oversee uniquely-focused clinical studies. Working...
Clinical Site Manager 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 As Clinical Site Manager you will be responsible for maximizing site performance and site engagement in our client...
Clinical Site Manager 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. As a Senior CRA / Clinical Site Manager you will be joining the world’s largest & most comprehensive clinical...
A global clinical research provider is seeking a Site Manager to oversee monitoring activities in clinical trials. Responsibilities include conducting site visits, ensuring regulatory compliance, and collaborating with study sites. The ideal candidate will have a Bachelor's and Master's degree in relevant fields, CRA certification, and experience in the pharma industry. Excellent English skills...
A leading pharmaceutical company seeks a Clinical Research Associate in Rome, Italy. This role includes managing site relationships, ensuring compliance with clinical trial protocols, and mentoring junior staff. Candidates should have a Bachelor’s degree and at least 1 year of clinical research experience. Strong interpersonal and collaboration skills are essential to effectively engage with...
A leading medical technology company is seeking a Senior Clinical Research Associate in Savona. The ideal candidate will be responsible for conducting on-site and remote monitoring visits while ensuring compliance with regulatory standards. Candidates should have a bachelor's degree in life sciences and at least 5 years of experience in clinical trial monitoring. This role offers a chance to work...
Research Nurse/Clinical Research Coordinator (Part-time, On-site, Independent Contractor) Novara Italy RapidTrials is hiring an experienced Clinical Research Coordinator (CRC) to support prescreening and recruitment activities for a Phase III MASH (Metabolic Dysfunction-Associated Steatohepatitis) clinical trial. This part‑time, freelance role is based in Novara. The role involves identifying...
Global Monitoring and Site Engagement (GMASE) Global Process Owner (GPO) – Clinical Operations GSK’s success absolutely depends on our people. While getting ahead of disease together is about our ambition for patients and shareholders, it’s also about making GSK a place where people can thrive. We want GSK to be a place where people feel inspired, encouraged and challenged to be the best they...
A global biopharmaceutical company is seeking a Clinical Research Associate in Rome, Italy. The role involves serving as the primary contact for investigative sites, conducting site evaluations, and ensuring compliance with protocols and regulations. Candidates should have at least a Bachelor's degree in a health-related field and 1+ years of clinical research experience. This position encourages...
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 global provider of clinical research services is seeking an Experienced Clinical Research Associate to monitor and manage clinical study sites based in Italy. The ideal candidate will have a Bachelor's degree and a Master's degree in a scientific field or health care, along with CRA certification. The role involves ensuring regulatory compliance, managing documentation, and maintaining...
A global biopharmaceutical company is seeking a Clinical Research Associate in Rome, Italy. The role involves serving as the primary contact for investigative sites, conducting site evaluations, and ensuring compliance with protocols and regulations. Candidates should have at least a Bachelor's degree in a health-related field and 1+ years of clinical research experience. This position encourages...
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...
A leading healthcare intelligence organization is seeking a Clinical Site Associate to support clinical trial operations in Milan. The role involves managing site communications, ensuring compliance, and maintaining documentation. Candidates should have a Bachelor's degree in life sciences or healthcare and experience in clinical research. Strong organizational skills, fluency in Italian and...
A leading medical device company is seeking a Senior Clinical Research Associate in Ascoli Piceno to conduct on-site and remote monitoring visits. The ideal candidate will have over 5 years of experience in clinical trial monitoring and strong knowledge of regulatory standards. Responsibilities include evaluating data accuracy, conducting monitoring visits, and ensuring compliance with safety...
A clinical research services firm is seeking a Clinical Research Associate in Milan, Italy. This position involves conducting site monitoring visits, ensuring compliance with regulations, and maintaining study documentation. A Bachelor's degree in a scientific discipline or healthcare, along with at least one year of clinical experience, is preferred. The ideal candidate will possess strong...
Clinical Site Associate 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. Clinical Site Associate (CSA) We are currently seeking a Clinical Site Associate (CSA) to join our diverse and...
Clinical Research Associate, Site Management - Italy Engage in a structured training program to gain knowledge and skills required to independently conduct clinical monitoring visits in accordance with study protocol, standard operating procedures, good clinical practice, and applicable regulatory requirements. Essential Functions - Complete appropriate therapeutic, protocol and clinical...
A medical device company located in Novara is seeking a Senior Clinical Research Associate. The ideal candidate should have at least 5 years of monitoring experience and be skilled in ensuring compliance with regulatory standards. Responsibilities include conducting on-site and remote monitoring visits, evaluating data accuracy, and providing training for clinical research personnel. This...
A global clinical research provider is seeking a Site Manager to oversee monitoring activities in clinical trials. Responsibilities include conducting site visits, ensuring regulatory compliance, and collaborating with study sites. The ideal candidate will have a Bachelor's and Master's degree in relevant fields, CRA certification, and experience in the pharma industry. Excellent English skills...