Join Our Team as a Clinical Director/Lead - Switzerland Are you a seasoned clinical development professional ready to lead groundbreaking therapies and shape the future of healthcare? We are seeking a dynamic Clinical...

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...

h3Clinical Trial Psych Rater - Italian Speaking /h3pLocation: Remote/Virtual /ppHours: Estimated 10–16 hours per month /ppRole: Clinical Specialist /ph3About IQVIA /h3pIQVIA is a global leader in advanced analytics,...

h3Nurse for Home Visits for clinical trial patients /h3pLocation: Padua Area /ppWeekly working hours: around 1-3h per week /ppVisits: weekly or every two weeks /ppContract duration: one year /ppIQVIA is hiring an...

ppOur clinical activities are growing rapidly, and we are currently seeking full-time, home or office-based Clinical Research Associates to join our Clinical Monitoring team in Italy. This position will work with a...

ppThe Clinical Research Associate position at Medpace offers the unique opportunity to have an bexciting career /b in the research of drug and medical device development while bmaking a difference /b in the lives of...

Clinical Independent Rater - Romanian Speaking Massimizzi le sue possibilità di successo assicurandosi che il suo CV e le sue competenze corrispondano ai requisiti di questa posizione. Location Remote/Virtual Hours:...

h3Clinical Trial Psych Rater - Italian Speaking /h3pLocation: Remote/Virtual /ppHours: Estimated 10–16 hours per month /ppRole: Clinical Specialist /ph3About IQVIA /h3pIQVIA is a global leader in advanced analytics,...

h3Clinical Research Coordinator in Milano /h3 h3Working Hours /h3 p20 hours per week /p h3Start Date /h3 pImmediately /p h3Duration /h3 pApproximately 6 months /p pIQVIA is currently recruiting a dedicated Clinical...

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...