Sede di lavoro: Rozzano (MI) Tipologia contrattuale: Contratto a Tempo Determinato Perché Humanitas Scegliere Humanitas significa entrare in un contesto in cui la qualità della cura si costruisce ogni giorno attraverso competenza clinica, innovazione e lavoro
The University of Tennessee Knoxville, College of Social Work, through the Social Work Office of Research and Public Service (SWORPS) is accepting applications for aCoordinatorforthe Tennessee Child Support Employment & Parenting Program (TCSEPP). Within SWORPS, the Tennessee
Locations: Milan, Italy Categories: Clinical Trial Management Req ID: 12806 Our clinical activities are growing rapidly, and we are currently seeking a full-time Clinical Trial Site Relationship Coordinator to join our vibrant Clinical Operations team in Italy,
Wood is recruiting for a Home Office Construction Engineer to join our Life Sciences division based in Milan, working on Pharmaceutical and Bio Tech projects across Europe and internationally. The position will be based in Corsico
Company Description The University of Notre Dame is more than a workplace; it is a vibrant, mission-driven community where every employee is valued and supported. Rooted in a tradition of excellence and inspired by our Catholic
DEADLINE FOR APPLICATIONS2 October 2026-23:59-GMT+01:00 Central European Time (Rome) WFP celebrates and embraces diversity. It is committed to the principle of equal employment opportunity for all its employees and encourages qualified candidates to apply irrespective of
Clinical Research Coordinator in Rome Working Hours: 2 hours per week Start Date : Immediately Duration : Approximately 6 months IQVIA is currently recruiting a dedicated Clinical Research Coordinator to support a clinical research site in Rome. This only 2 hour
IQVIA in Rome, Lazio, seeks a part-time Clinical Research Coordinator for field-based work. The role involves prescreening, data review, and documentation, with a focus on patient screening, consent, and study logistics. You’ll collaborate with monitors and sites to ensure
Rome, Italy | Part time | Field-based | R1568090 Clinical Research Coordinator in Rome Working Hours: 2 hours per week Start Date: Immediately Duration: Approximately 6 months Key Responsibilities Prescreening and Screening tasks Review charts from the site
Rome, Roma, Italy Part time R1568090 Clinical Research Coordinator in Rome Working Hours: 2 hours per week Start Date : Immediately Duration : Approximately 6 months IQVIA is currently recruiting a dedicated Clinical Research Coordinator to support a clinical research site
IQVIA is recruiting a Clinical Research Coordinator to support a site in Rome, Italy. This part-time role requires approximately 2 hours per week and starts immediately, for a duration of about 6 months. You will prescreen, review charts,
Sede di lavoro : Humanitas San Pio X - Milano Tipologia contrattuale : tempo determinato (12 mesi) – full time Scegliere Humanitas significa entrare in un contesto in cui la qualità della cura si costruisce ogni
Job Overview:The Senior Clinical Research Associate II (Sr CRA II) is responsible and accountable for site monitoring and site management for clinical studies according to Fortrea, and/or Sponsor, Standard Operating Procedures, and Regulatory Guidelines. The Sr CRA II
Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life -
We are looking for a motivated Clinical Research professional to join our Clinical Operations team. This role is designed for someone with a scientific/life sciences degree and initial experience in clinical research, such as a Clinical Trial Assistant
Clinical Research Associate I (CRA I) – Italy Location: Italy Working arrangement: Home-based with travel to clinical trial sites Employment type: Full-time, permanent The Opportunity We are partnering with an international clinical research organisation seeking a Clinical Research Associate
Work ScheduleStandard (Mon-Fri) Environmental ConditionsOffice Job Description Join Us as a Clinical Trial Coordinator – Make an Impact at the Forefront of Innovation What Youll Do Clinical Trial & Documentation Support Coordinate and complete assigned clinical trial
Medpace is currently seeking candidates with PhDs and/or Post-Doctoral Research experience for a full-time, office-based Associate Clinical Trial Manager (aCTM) to join our Clinical Trial Management team. The aCTM will be a part of the Clinical Trial
Job Overview The medical department consists of a Chief Medical Officer, Medical Directors, Sr Medical Directors, Medical Writers, and Safety Associates. The Medical Director provides medical and scientific support to clinical research programs, study teams and investigators. The
Company Description The University of Notre Dame is more than a workplace; it is a vibrant, mission-driven community where every employee is valued and supported. Rooted in a tradition of excellence and inspired by our Catholic