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...
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...
POSITION SUMMARY 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 Naples. The role involves identifying potential participants, engaging referral sources, coordinating prescreening, assisting...
POSITION SUMMARY 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 Naples. The role involves identifying potential participants, engaging referral sources, coordinating prescreening, assisting...
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...
Position Summary POSITION SUMMARY 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 Naples. The role involves identifying potential participants, engaging referral sources, coordinating...
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 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 global clinical research organization is looking for a Clinical Contract Specialist based in Italy. The role involves preparing and negotiating site contracts, monitoring timelines, and serving as the main contact for Clinical Trial Agreements. Ideal candidates will hold a Bachelor's degree and have at least one year of relevant experience in clinical trials within Italy. Fluency in both...
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 leading Pharma company in Florence is seeking a Senior Clinical Research Associate with over 10 years of experience, ideally in ATTR cardiac amyloidosis. Responsibilities include ensuring compliance with regulations, conducting monitoring visits, and supporting investigator site teams. This role offers a unique opportunity to work on important studies in a dynamic environment, with...
A leading pharmaceutical company in Florence is seeking a Senior Clinical Research Associate to ensure compliance with regulations and support site teams. The ideal candidate will have over 10 years of experience, ideally in ATTR cardiac amyloidosis or non-interventional studies. This role involves site initiation, monitoring, data accuracy, and supporting patient recruitment. Interested...
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...
Position Summary 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 Naples. The role involves identifying potential participants, engaging referral sources, coordinating prescreening, assisting...
Job Overview Engage in 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 research training to perform job duties. • Gain...
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...
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...
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 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 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...