Un importante istituto di ricerca clinica cerca un case manager per la gestione di pazienti emicranici. Il candidato ideale avrà una laurea in scienze mediche e sarà coinvolto nella gestione di trial clinici. Le responsabilità includono l'interazione con medici e CRO, la gestione degli studi clinici e lo sviluppo di progetti di ricerca. È richiesta una buona conoscenza dell'inglese e competenze...
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...
A leading life sciences company in Italy seeks a Clinical Study Administrator to coordinate study activities and manage trial documentation in compliance with regulatory standards. The ideal candidate will have a Bachelor’s degree in a related field, along with at least 2 years of relevant experience. Strong collaboration, organizational skills, and proficiency in MS Office are essential. The...
A renowned Contract Research Organization in Milan is seeking a Clinical Trial Assistant to support project execution from start to finish. The ideal candidate will have a Master’s Degree in a scientific discipline or health care, possess strong organizational and decision-making skills, and be fluent in English. This role involves managing study documents, evaluating study sites, and...
A biotech-focused CRO in Italy is seeking a Clinical Research Associate (CRA) to coordinate and oversee clinical studies, ensuring compliance with protocols and regulations. The ideal candidate should have a degree in a scientific field and up to 12 months of experience as a CRA. Responsibilities include site monitoring, interaction with regulatory teams, and managing study materials. This role...
A leading biotech CRO in Italy is seeking a Clinical Research Associate (CRA) to coordinate clinical studies and ensure compliance with protocols. The ideal candidate will possess a degree in a scientific field, preferably with some experience in clinical research. Responsibilities include conducting feasibility studies, monitoring sites, and ensuring data accuracy. Competitive salary and...
Clinical Study Unit Intern Milan, Italy About the job Looking to launch your career at the cutting edge of healthcare? Join Sanofi for a chance to develop with mentoring and guidance from inspirational leaders while helping to make an impact on the lives of countless people worldwide. As Clinical Study Unit Intern , you'll have the chance to support key roles in clinical trial management and...
A leading Contract Research Organization is looking for a Study Project Manager in Milano, Italy. The role involves managing clinical trial activities and coordinating teams to ensure successful project execution. Candidates should hold a scientific degree and possess excellent communication and organizational skills. Experience with CTMS tools is a plus. This role requires leading regulatory...
L'IRCCS Ospedale San Raffaele (OSR), struttura clinica-scientifica-universitaria di rilievo internazionale e di alta specializzazione per diverse importanti patologie, sta ricercando un Study Coordinator/Data Manager da inserire nella propria Unità/Laboratorio URI-Urological Research Institute. Attività principali - Gestione di database di pazienti: raccolta, data entry e collaborazione...
Il Gruppo Humanitas, riferimento di eccellenza per la salute, la prevenzione e la diagnosi, è presente in Italia con 11 ospedali ad alta specializzazione, 24 Medical Care - la nostra rete di centri medici e punti prelievo, un Centro di Ricerca e Humanitas University, ateneo internazionale dedicato alle life sciences. Ogni anno, oltre 1.300.000 pazienti scelgono di affidarsi agli specialisti...
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 hub—coordinating study activities, maintaining study...
Un ospedale di eccellenza in Lombardia cerca un Data Manager per gestire le proposte di studio e coordinare tutte le fasi operative. Il candidato ideale ha una laurea in ambito scientifico e un'ottima conoscenza dell'inglese, oltre a competenze informatiche. È fondamentale un anno di esperienza nel ruolo, preferibilmente in oncologia. L'ospedale offre un contratto a tempo determinato di un anno e...
A biotech-focused CRO in Italy is seeking a Clinical Research Associate (CRA) to coordinate and oversee clinical studies, ensuring compliance with protocols and regulations. The ideal candidate should have a degree in a scientific field and up to 12 months of experience as a CRA. Responsibilities include site monitoring, interaction with regulatory teams, and managing study materials. This role...
Clinical Study Administrator (CSA) within Country Operations Management (COM) Responsible for coordinating study activities from start‑up to execution and close‑out, ensuring quality and consistency in trial deliverables and meeting time, cost, and quality objectives in accordance with Good Clinical Practice (GCP), Alexion Standard Operating Procedures (SOPs), and evolving regulatory...
A clinical research company is seeking a detail-oriented Central Study Coordinator for a part-time position in Italy. The role involves supporting the planning and coordination of clinical studies, maintaining documentation, and ensuring compliance with regulatory standards. Candidates should have a Bachelor’s in Life Sciences and GCP knowledge, with preferred experience as a CRA or CTA. This...
Clinical Study Administrator (CSA) within Country Operations Management (COM) Responsible for coordinating study activities from start‑up to execution and close‑out, ensuring quality and consistency in trial deliverables and meeting time, cost, and quality objectives in accordance with Good Clinical Practice (GCP), Alexion Standard Operating Procedures (SOPs), and evolving regulatory...
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 hub—coordinating study activities, maintaining study...
A clinical research company is seeking a detail-oriented Central Study Coordinator for a part-time position in Italy. The role involves supporting the planning and coordination of clinical studies, maintaining documentation, and ensuring compliance with regulatory standards. Candidates should have a Bachelor’s in Life Sciences and GCP knowledge, with preferred experience as a CRA or CTA. This...
A leading life sciences company in Italy seeks a Clinical Study Administrator to coordinate study activities and manage trial documentation in compliance with regulatory standards. The ideal candidate will have a Bachelor’s degree in a related field, along with at least 2 years of relevant experience. Strong collaboration, organizational skills, and proficiency in MS Office are essential. The...
Are you ready to make a difference in the world of clinical trials? As a Clinical Study Administrator (CSA) within Country Operations Management (COM), you'll play a pivotal role in coordinating study activities from start-up to execution and close-out. Your mission is to ensure quality and consistency in trial deliverables, meeting time, cost, and quality objectives according to Good Clinical...