Hybrid Clinical Site Associate – Milan, TMF

Clinical Site Associate, office based hybrid, Warsaw, Poland ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, pintar you to join us on our mission to shape the future of clinical development. Clinical Site Associate (CSA) We are...

Clinical Site Associate 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. Clinical Site Associate (CSA) We are currently seeking a Clinical Site...

A leading healthcare intelligence organization is seeking a Clinical Site Associate to support clinical trial operations. The role requires managing site communications, coordinating trainings, and maintaining essential documentation. Ideal candidates will have a Bachelor's in life sciences, experience in clinical research, and strong organizational skills....

A leading Contract Research Organization is seeking a Trial Master File Associate to manage the Trial Master File (TMF). The role involves organizing and maintaining TMF compliance according to regulations and collaborating with study teams. Ideal candidates have TMF management experience and a Bachelor's degree in Health Science. This position offers...

A Contract Research Organization in Lombardy seeks a full-time Clinical Research Associate to manage clinical trials and ensure compliance with protocols. The individual will be responsible for conducting site visits, collaborating with clinical teams, and verifying data accuracy. Candidates must have at least 2 years of relevant experience, a degree in Life...

A global healthcare-focused organization is seeking a Trial Master File Associate to manage the Trial Master File in a flexible hybrid work model. The role requires at least 3 years of experience in TMF management, preferably within ophthalmology, and a degree in a related field. Responsibilities include organizing TMF documentation, training study teams,...

A Contract Research Organization located in Milan is seeking a full-time Clinical Research Associate. This role involves monitoring clinical trials, ensuring protocol adherence, and managing data accuracy. Candidates should have a Bachelor’s or Master’s degree in Life Sciences, with at least two years of experience in interventional studies. Proficiency...

Company Description Phidealive, established in 2018, is a Contract Research Organization (CRO) with a strong foundation in Italy’s rich clinical research culture. Positioned as a Clinical Research Atelier, Phidealive emphasizes scientific rigor, regulatory compliance, and a tailored operational approach for each project. The company collaborates with...

A global Contract Research Organization is seeking a Trial Master File Associate to work remotely or hybrid. The role involves managing the Trial Master File and ensuring compliance with TMF processes. The candidate should have 1-5 years of relevant experience, preferably in CRO or Pharmaceutical sectors, and must demonstrate strong organizational skills and...

Overview CLINICAL RESEARCH ASSOCIATE - REMOTE BASED (ITALY) TFS HealthScience is a leading global, mid-size Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies throughout their entire clinical development journey. Our expertise includes full service-capabilities, resourcing and functional service (FSP)...