A global biopharma company is looking for a Study Manager to coordinate clinical studies from planning to close-out. This role requires strong communication and project management skills and offers a hybrid work model. Candidates should have at least 3 years of experience in the pharmaceutical field and a deep understanding of clinical trial regulations. Enjoy benefits including flexible working...
Direct message the job poster from Philogen S.p.A. Philogen S.p.A. is a biotechnology company whose mission is the development of biologic products for the imaging and therapy of life‑threatening diseases, with a strategic focus on cancer diseases and rheumatologic disorders. Philogen S.p.A. would like to hire a highly motivated and qualified Clinical Data Manager who will report to the Data...
Philogen S.p.A., a biotech company listed on the Milan Stock Exchange and a leader in the development of innovative anti-tumor therapies, is expanding its clinical activities and will be opening a new office in Milan . Philogen S.p.A. would like to hire a CLINICAL RESEARCH ASSOCIATE for the development of clinical experimental activity. The successful candidate will have responsibility for...
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...
A leading company in the pharmaceutical sector is seeking a Senior Clinical Research Associate in Florence, Italy. The ideal candidate will have over 10 years of experience in clinical research, preferably with knowledge in ATTR cardiac amyloidosis and non-interventional studies. The role involves ensuring compliance with study protocols, monitoring visits, managing regulatory documentation, and...
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...
Join to apply for the Clinical Quality Assurance Associate role at Kedrion Biopharma Join to apply for the Clinical Quality Assurance Associate role at Kedrion Biopharma Get AI-powered advice on this job and more exclusive features. Department: Global Quality Systems and Compliance Position Overview: We are seeking a motivated and dynamic individual to join our Global Quality Systems and...
Remoto EUR 30.000 - 50.000 2 giorni fa If you are an experienced CRA who is passionate about oncology research and looking to join a highly skilled and knowledgeable team, TRIO is the place for you! Translational Research in Oncology (TRIO) is a global clinical research organization dedicated to advancing translational cancer research in the clinical trial setting. Our passionate team is...
Overview TRIO is looking for a Clinical Research Associate to join our Monitoring Resources team. Reporting to a CRA Line Manager, this position will be home-based in Italy. Translational Research in Oncology (TRIO) is a global clinical research organization dedicated to advancing translational cancer research in the clinical trial setting. Our passionate team is committed to providing cancer...
If you are an experienced CRA who is passionate about oncology research and looking to join a highly skilled and knowledgeable team, TRIO is the place for you! Translational Research in Oncology (TRIO) is a global clinical research organization dedicated to advancing translational cancer research in the clinical trial setting. Our passionate team is committed to providing cancer treatments of...
Social network you want to login/join with: Senior Clinical Research Associate, siena col-narrow-left Client: Teleflex Location: Job Category: Other - EU work permit required: Yes col-narrow-right Job Reference: 8556790222002585600337159 Job Views: 2 Posted: 27.08.2025 Expiry Date: 11.10.2025 col-wide Job Description: POSITION SUMMARY: The Senior Clinical Research Associate...
As Study Manager you will lead and coordinate the delivery of clinical and evidence generation studies from planning through close-out. You will work with study teams, vendors, and country colleagues to keep studies on time, on budget, and compliant with standards. We value clear communication, practical problem solving, and a focus on quality. This role offers growth through exposure to global...
Overview 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 14155, 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...
EUR 60.000 - 80.000 2 giorni fa 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),...
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...
A global biopharma company is looking for a Study Manager to coordinate clinical studies from planning to close-out. This role requires strong communication and project management skills and offers a hybrid work model. Candidates should have at least 3 years of experience in the pharmaceutical field and a deep understanding of clinical trial regulations. Enjoy benefits including flexible working...
Social network you want to login/join with: Senior Clinical Research Associate, Prato Client: Teleflex Location: Prato, Italy Job Category: Other EU work permit required: Yes Job Reference: 8556790222002585600337140 Job Views: 2 Posted: 27.08.2025 Expiry Date: 11.10.2025 Job Description: POSITION SUMMARY: The Senior Clinical Research Associate (Senior CRA) is responsible for scheduling...
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...
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...
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...