Clinical Research Associate

Evidilya, CRO digital-native del Gruppo SPRIM., che Progetta e conduce studi interventistici e Real-World Evidence su scala globale nei settori Pharma, Consumer Healthcare, Medical Devices e Food & Nutrition Massimizzi le sue possibilità di successo assicurandosi che il suo CV e le sue competenze corrispondano ai requisiti di questa posizione.

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 work to ensure that sites are conducting the study(ies) and...

Planet Pharma are currently partnered with an exciting global CRO and we are actively seeking an experienced Clinical Research Nurse to join the business on a freelance basis. This is an ad-hoc role in Brescia. Key Responsibilities: Conducting home visits to patients taking part in clinical trials Conduct patient assessments, including recording vital...

Fondazione Telethon is a major Italian charity focused on rare genetic diseases. Founded in 1990, its mission is to advance biomedical research towards the cure of genetic diseases with the ultimate goal of making new therapies available to patients in need. Fondazione Telethon has 3.186 projects for an overall amount of 790 million Euro , both within its...

Overview In this role you support regional clinical study delivery to ensure trials run on time, within budget, and to quality standards. You collaborate with the Regional Clinical Study Manager, global teams, and site staff to coordinate feasibility, start-up, TMF, and site communications. You gain hands-on experience in clinical operations and regulatory...

Overview In this role, you will lead site management and monitoring for assigned trials to ensure patient safety and high-quality execution. You will work with cross-functional teams to keep study activities on track from activation to database lock. You will monitor AEs/SAEs and support Drug Safety, audits, and CAPA implementation. This is a remote,...

PSI is a leading Contract Research Organization with 30 years experience in the industry, offering a perfect balance between stability and innovation to both clients and employees. We focus on delivering quality and on-time services across a variety of therapeutic indications. Take your career to the next level and lead challenging full-service global...

Overview In this role you support regional clinical study delivery to ensure trials run on time, within budget, and to quality standards. You collaborate with the Regional Clinical Study Manager, global teams, and site staff to coordinate feasibility, start-up, TMF, and site communications. You gain hands-on experience in clinical operations and regulatory...

PSI CRO is seeking an experienced Clinical Project Manager to lead challenging full-service global clinical research projects, managing the full scope from startup to closure and hands-on involvement in every aspect of the study.Remote or Hybrid work is supported. You will bring recent clinical research experience in project management, global/regional...