On behalf of our Client - Chiesi Farmaceutici, one of the top 50 pharmaceutical companies in the world, with more than 80 years of experience within the pharmaceutical and biotechnology industry a global pharmaceutical company - IQVIA is looking for a eTMF Specialist who can join an exciting working environment in a dynamic atmosphere. This position will oversee the global eTMF (electronic Trial...
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...
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...
CPL & TAYLOR by Synergos is recruiting: CLINICAL BUSINESS PARTNER LIFE SCIENCES (Ref. ANN417222) 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 supports...
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...
Veeda Lifesciences is seeking a Clinical Research Associate (CRA) based in Italy for its growing international hematology/oncology Clinical Trials program. This is a full-time job. Job overview: The CRA is responsible for ensuring that the conduct of a clinical trial at selected Investigational Sites is according to the currently approved protocol/amendments, ICH GCP guidelines, the applicable...
Location: Siena - Italy Department: Clinical About Philogen Philogen S.p.A. is a biotechnology company dedicated to developing targeted products for the imaging and treatment of life-threatening diseases, with a strategic focus on oncology. Our mission is to translate cutting-edge scientific innovation into effective therapies that improve patients' lives. Position Overview In preparation for the...
Job Title: Clinical Quality Assurance Specialist (GCP) Location: Siena - Italy Department: Clinical About Philogen Philogen S.p.A. is a biotechnology company dedicated to developing targeted products for the imaging and treatment of life-treating diseases, with a strategic focus on oncology. Our mission is to translate cutting-edge scientific innovation into effective therapies that improve...
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...
Philogen is looking for a " Clinical Quality Assurance Specialist (GCP)". The position will be responsible to assess compliance with SOPs, Gx P, 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...
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...
Upsilon Global are seeking a freelance CRA based in Italy to perform remote monitoring visits and site management activities across 5 sites for a cardiology study. This is estimated to be 0.5 FTE, starting in October and working with an expanding CRO with operations across US, EU and APAC regions. Regulatory and start-up activities have been performed and we now need a local expert to take over...
Director, Product Strategy & Innovation Posted Date: Jan 9 2026 Job Purpose This role requires deep understanding of both the clinical trial landscape as well as Product Development methodologies and systems‑thinking, with a unique mix of domain knowledge, process expertise, problem framing skills, product management discipline, and technology acumen to ensure successful delivery. Key...
CPL & TAYLOR by Synergos is recruiting:CLINICAL BUSINESS PARTNERLIFE SCIENCES(Ref. ANN417222)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 pharmaceutical and...
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...
On behalf of our Client - Chiesi Farmaceutici, one of the top 50 pharmaceutical companies in the world, with more than 80 years of experience within the pharmaceutical and biotechnology industry a global pharmaceutical company - IQVIA is looking for a eTMF Specialist who can join an exciting working environment in a dynamic atmosphere. This position will oversee the global eTMF (electronic Trial...
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...
A leading medical device company is seeking a Senior Clinical Research Associate in Siena, Italy. This role involves conducting monitoring visits, ensuring compliance with regulatory standards, and providing leadership in clinical studies. The ideal candidate should have over 5 years of experience in clinical trial monitoring, strong attention to detail, and excellent communication skills. This...