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
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
CRA I Syneos Health® is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators at every point across the drug development and commercialization continuum, helping them navigate complexity, anticipate
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
Are you passionate about clinical research and driven by the opportunity to bring life-changing therapies closer to patients? We are looking for a Clinical Research Associate I to join Novo Nordisk Italy on a maternity cover
Sponsor Dedicated Sr CRA - Phase I Oncology - Based Rome Area Syneos Health® is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators at every point across the
Sponsor Dedicated CRA II/Sr CRA I/II - Home Based ITA Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes
Job Overview: Site monitoring and site management responsibility for clinical studies according to Company, and/or Sponsor, Standard Operating Procedures, and Regulatory Guidelines for the Unblinded model. Assures the implementation of project plans, as assigned. Summary of
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
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
This job is with Thermo Fisher Scientific, an inclusive employer and a member of myGwork – the largest global platform for the LGBTQ+ business community. Please do not contact the recruiter directly. Work Schedule Standard (Mon-Fri)
Trial Delivery Leader (TDL) The Trial Delivery Leader (TDL) serves as the single point of accountability for trial operational strategy, trial‑level budget, quality, and on‑time delivery of assigned clinical trials. This role represents the evolution of the Global Trial Leader (GTL), with
Specialist, Clinical Trial Management The Specialist, Clinical Operations supports the planning, execution, and administration of clinical trials. This position is responsible for administrative and coordination tasks and will have increasing Study Team Lead (STL) accountabilities with oversight of
Evidilya , la Contract Research Organization dedicata di Sprim Health Group, opera come realtà full-service con competenza internazionale nello sviluppo e nella gestione di studi osservazionali, pre-clinici e clinici, ricerca un/una: per rafforzare il nostro Team
Evidilya, realtà italiana di Sprim Health Group, cerca una figura per rafforzare il Team Operativo di Milano. La posizione prevede collaborazione con il team di studio dallinizio alla fine, gestione documentale e sviluppo del Trial Master File. Si richiede
Job OverviewPerform 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 sponsor requirements.Essential Functions:• Perform site monitoring
Job OverviewPerform 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 sponsor requirements.Essential Functions• Perform site monitoring
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 of study
At Allucent, we are dedicated to helping small‑medium biopharmaceutical companies efficiently navigate the complex world of clinical trials to bring life‑changing therapies to patients in need across the globe. Responsibilities Leads the project team, ensuring the project
Clinical Research Associate, Site Management - Italy page is loaded# Clinical Research Associate, Site Management - Italylocations: Milan, Italy: Milan, Italytime type: Full timeposted on: Posted Todayjob requisition id: R1540967Job Overview Perform monitoring and site management