Area di lavoro: Triveneto e Lombardia Residenza: Idealmente in Veneto Lazienda Siamo a metà degli anni ‘50: per la prima volta una paziente con stomia può indossare una sacca adesiva in plastica che le permette di
Area di lavoro: Emilia-Romagna, Marche, Umbria, Molise e Abruzzo. Residenza: Idealmente in Emilia-Romagna Lazienda Siamo a metà degli anni ‘50: per la prima volta una paziente con stomia può indossare una sacca adesiva in plastica che
Why Orthofix? Guided by our organizational values – Take Ownership | Innovate Boldly | Win Together – we collaborate closely with world-class surgeons and other partners to improve people’s quality of life. At Orthofix, we want
Alira Health S.r.l. in Verona, Italy, is seeking a Clinical Trial Coordinator to assist the clinical research team in conducting studies in accordance with regulations and timelines. Responsibilities include managing start-up activities, documentation, and invoicing.The ideal candidate will
# Clinical Trial CoordinatorApplyremote type: Hybridlocations: Verona: Verona-Remotetime type: Full timeposted on: Posted Todayjob requisition id: JR000583 Are you being referred to one of our roles by a connection in Alira Health? If so, please apply using
Experteer Italy is looking for a professional to lead site management and monitoring for clinical trials, ensuring patient safety and high-quality execution. The role involves working with cross-functional teams from activation to database lock.Applicants should have a
Experienced Clinical Research Associate, IQVIA Biotech - Home based, Italy 1 day ago Be among the first 25 applicants Job Overview Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting
Senior French Prompt Engineer – Clinical AI / LLM | Remote in EuropeWe are looking for a Senior French-speaking Prompt Engineer / Applied Research Scientist to contribute to the development of AI-powered clinical documentation systems.In this role, you will
The Sr CRA is an important member of the Alira Health Clinical team. The Sr CRA is highly motivated and functions independently to conduct site monitoring responsibilities for clinical trials; as well as providing oversight, leadership, and guidance
The Sr CRA is an important member of the Alira Health Clinical team. The Sr CRA is highly motivated and functions independently to conduct site monitoring responsibilities for clinical trials; as well as providing oversight, leadership, and guidance
A global healthcare solutions company in Italy is seeking a Sr Clinical Research Associate. The role involves conducting site monitoring for clinical trials, ensuring protocol compliance, and providing leadership in managing clinical trials. Candidates should have a minimum of
Are you being referred to one of our roles by a connection in Alira Health? If so, please apply using the referral link emailed to you. Join our global team dedicated to innovation and initiative, where
Job SummarySenior Chief Research Associate (Sr CRA) based in Italy, responsible for independent site monitoring, oversight, and management of clinical trials to ensure compliance with protocols, GCP, and sponsor requirements. Works closely with US and EU monitoring
Job Description Our Clinical Research and Pharmacovigilance team push the boundaries of global healthcare through research and innovation. Through clinical trials and surveillance, we ensure the safety and efficacy of our existing and pipeline products to produce safe,
Experienced Clinical Research Associate, IQVIA Biotech - Home based, Italy Scopra di più su questo ruolo leggendo le informazioni qui sotto, quindi invii la sua candidatura per essere preso/a in considerazione. 1 day ago Be among the
Experienced Clinical Research Associate, IQVIA Biotech - Home based, Italy Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and
Clinical Account Manager – Italy Location: Home-based, Italy Territory: Italy Travel: Approximately 50% The Opportunity Im currently supporting an innovative international life sciences organisation as it continues to strengthen its commercial team across Europe. This is an
A leading consulting firm is seeking a Senior French-speaking Prompt Engineer capable of contributing to the development of AI-powered clinical documentation systems. In this role, you will design and optimize prompts for large language models focused on healthcare
Medpace is the leading CRO for Biotech companies and is continuing to add Clinical Trial Managers of different experience levels to join our Clinical Trial Management Group in our Milan office. Clinical Trial Managers with expertise in Immunology and
Job Description SummaryThe Clinical Trial Coordinator assists the clinical research team, ensuring the study is conducted in accordance with GCP, SOP, protocol, and respecting budget and timelines. The Coordinator manages start-up activities and documents management.Key ResponsibilitiesResponsible (under PM