Job Overview 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 guidelines, and...

Mandarin oriental, Milan is looking for a SPA Therapist to join our SPA team. Are you a master of craft?Do you thrive in a team that succeeds together, demonstrating integrity and respect while acting responsibly? Do...

Nurse for Home Visits for clinical trial patients Location: Padua Area Weekly working hours: around 1-3h per week Visits: weekly or every two weeks Contract duration: one year IQVIA is hiring an experienced Clinical...

About Tia Tia is building a new model for women's healthcare, one that treats women as whole people, not separate conditions or life stages. By integrating primary care, mental health, gynecology, dermatology, and...

Clinical Research Coordinator in Milano Working Hours 20 hours per week Start Date Immediately Duration Approximately 6 months IQVIA is currently recruiting a dedicated Clinical Research Coordinator to support a...

This position is listed on behalf of a partner company, who manages all applications and next steps. Our partner is looking for a Clinical Site Payment Associate Manager based in Italy. As a Clinical Site Payment...

Job Description Summary The International Clinical Education & Strategy CVUS manager is responsible for defining and executing the clinical education and alignment strategy across regions in close collaboration with...

Premier Research is seeking a Senior Clinical Research Associate / CRA II to join our Clinical Monitoring, Site Management and SSU team. You will monitor sites, ensure data integrity and patient safety, and prepare...

Syneos Health is seeking a Sponsor Dedicated CRA II/Sr CRA I/II for home-based work in ITA. The role supports site qualification, monitoring and data management for oncology trials, with up to 75% travel. Strong...

Syneos Health, Inc. is seeking a CRA II Italia - Home Based to support site qualification, initiation, monitoring and close-out visits. You will ensure regulatory compliance, verify informed consent, and protect...