Job Overview: Site monitoring and site management responsibility for clinical studies according to Company, and/or Sponsor, Standard Operating Procedures, and Regulatory Guidelines. Assures the implementation of project plans, as assigned. Summary of Responsibilities: Responsible for all aspects
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 activities in accordance
Clinical Trial Administrator (Fixed Term, One Year Contract) Research & Development, Clinical Development Centre Italy Rome, Italy Every clinical trial that reaches patients depends on meticulous coordination behind the scenes. Join us in Rome and be the person who
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) solutions. Join Our
Clinical Research Associate ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the
Clinical Research Associate II/Senior Clinical Research Associate/ CRA/Sr CRA/ Italy - Milan, Rome, Bologna, Naples ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As
Who we are We’re a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world’s most persistent diseases is not paved by those who play it safe. It
Parexel is seeking an experienced Medical Writer to join a sponsor-aligned program supporting one of our key sponsors. You will deliver medical writing services for CTRs, CTPs, amendments, IBs and submission documents, collaborating closely with project
Category:RN City:Milan State:Tennessee Shift:12 - Evening (United States of America) Job Description Summary:Under the general supervision of the Director and Clinical Manager, responsible for providing quality patient care using the nursing process, the direction of other nursing
Perché Ascom? Ascom sviluppa soluzioni software ICT e workflow clinici utilizzati in oltre 12.000 ospedali nel mondo, supportando attività mission-critical in contesti come Terapie Intensive, Sale Operatorie, Pronto Soccorso e sistemi di comunicazione ospedaliera. Le soluzioni
Job ID 515837 Posted since 31-Jul-2026 Organization Siemens Healthineers Field of work Quality Management Company ADVANCED ACCELERATOR APPLICATIONS MOLECULAR IMAGING ITALY S.R.L. Experience level Mid-level Professional Job type Full-time Work mode Office/Site only Employment type Permanent
IT Vendor Performance & PMO Analyst At Fresenius Medical Care, we are the global leader in kidney care, committed to improving the lives of patients with chronic kidney disease. Our mission is to deliver high-quality, innovative
Work ScheduleStandard (Mon-Fri) Environmental ConditionsAdherence to all Good Manufacturing Practices (GMP) Safety Standards, Office, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.) Job Description How will you
Work ScheduleStandard (Mon-Fri) Environmental ConditionsOffice Job Description Were looking for a Clinical Research Associate II (CRA II) to join our growing Clinical Operations team in Italy. If youre passionate about clinical research, enjoy building strong site relationships, and want
Category:RN City:Milan State:Tennessee Shift:12 - Day (United States of America) Job Description Summary:Under the general supervision of the Director and Clinical Manager, responsible for providing quality patient care using the nursing process, the direction of other nursing
We are looking for individuals who want to join our team in Vicenza, Italy. Apply now! Job Opportunity: New Parent Support Program Home Visitor Location: Vicenza, Italy Start Date: Immeditely Schedule: Full Time Make a Difference
Senior Clinical Reseacrh Associate ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven organisation, integrity, collaboration, agility, and inclusion are at
As part of the HSM team, be responsible for intake/approvals for biospecimen sourcing (global sourcing). Ensures Service Level Agreement (SLA) delivery and alignment with global standards. This role entails : Support the local SLA process Manage
Work ScheduleStandard (Mon-Fri) Environmental ConditionsOffice Job Description Join Us as an Assistant Clinical Research Associate – Make an Impact at the Forefront of Innovation What Youll Do Study & Site Support Complete assigned study and site management
Internal Employees: Please ensure that you are logged into Workday and applying through the Jobs Hub before proceeding.Certified Medical Assistant - Bonutti Occupational Medicine Job Description Certified Medical Assistant are responsible for providing assistance to providers