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...
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...
Join to apply for theHead, Global Study Managementrole atGSK Site Name:Warsaw, Belgium-Wavre, Bengaluru, Luxor North Tower, Italy - Siena, Mississauga Milverton Drive, UK – London – New Oxford Street, USA - Pennsylvania - Upper Providence Posted Date:Oct Company Overview At GSK, we have bold ambitions for patients, aiming to positively impact the health of 2.5 billion people by the end of the...
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...
Overview 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 rheumathologic disorders. Philogen S.p.A. would like to hire a highly motivated and qualified Clinical Data Manager who will report to the Data Manager Coordinator. Responsibilities Perform...
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...
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...
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...
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...
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...
CPL & TAYLOR by Synergos is recruiting: SENIOR DIGITAL CLINICAL CONSULTANT LIFE SCIENCES (Ref. ANN418147) LOCATION: Full remote CONTRACT: Permanent, full-time COMPENSATION: To be defined based on experience The Company A leading international organization specializing in consulting and digital solutions for the Life Sciences sector, headquartered in Italy. Founded in 2010, the company...
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...
Philogen is looking for a "Clinical Quality Assurance Specialist (GCP)". The position will be responsible to assess compliance with SOPs, GxP, European regulations, local regulations and guidelines, and clinical study protocols. This position will collaborate with other functions in the Clinical Department. In particular the successful candidate will be responsible to: Maintain GCP/ICH compliant...
Precision for Medicine is not your typical CRO. We are passionate about cultivating our culture and are proud to share extremely high CRA retention rates compared to industry averages. CRAs join us, love their jobs, and stay because of the amazing people and enjoyable quality of life. You will focus on an average of one to two studies setting you up to be a protocol expert. Travel is reasonable...
Philogen is looking for a "Clinical Quality Assurance Specialist (GCP)". The position will be responsible to assess compliance with SOPs, GxP, European regulations, local regulations and guidelines, and clinical study protocols. This position will collaborate with other functions in the Clinical Department. In particular the successful candidate will be responsible to: - Maintain GCP/ICH...
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...
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,...
CPL & TAYLOR by Synergos, ricerca: JUNIOR CLINICAL CONSULTANT – LIFE SCIENCES (Rif. ANN425949) SEDE DI LAVORO: Si valutano profili provenienti da tutta Italia, full remote. Sedi aziendali a Verona, Milano, Roma CONTRATTO: Tempo indeterminato, full time RETRIBUZIONE: da concordare L'azienda Importante realtà internazionale specializzata in consulenza e soluzioni digitali per il settore Life...
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...
CPL & TAYLOR by Synergos is recruiting:SENIOR DIGITAL CLINICAL CONSULTANTLIFE SCIENCES(Ref. ANN418147)LOCATION: Full remoteCONTRACT: Permanent, full-timeCOMPENSATION: To be defined based on experienceThe CompanyA leading international organization specializing in consulting and digital solutions for the Life Sciences sector, headquartered in Italy. Founded in 2010, the company supports...