Offerte di lavoro clinical study coordinator – Torino

Auxologico è alla ricerca di un/aCase Management con gestione e presa in carico dei Pazienti emicranici in concerto con medici ed infermieri nell’ambito del team di ricerca clinica del centro Trial Clinici. Attività e responsabilità: Gestione degli studi clinici interventistici ed osservazionali. Interazione con promotore e direzione scientifica...

Based in Rome, Novo Nordisk A/S is seeking a Clinical Trial Administrator to keep Italy’s trials moving with accuracy and pace. You will support the local study team from start-up to close-out, managing trial documentation, tracking progress, coordinating vendors and ensuring timely investigator site payments.You will work within the Business Operations...

Auxologico è alla ricerca di un/a Case Management con gestione e presa in carico dei Pazienti emicranici in concerto con medici ed infermieri nell'ambito del team di ricerca clinica del centro Trial Clinici.Attività e responsabilità:Gestione degli studi clinici interventistici ed osservazionali. Interazione con promotore e direzione scientifica...

Provide support to Clinical Affairs team to assure study site selection and conduct of the study by study sites in compliance with Good Clinical Practices, federal regulations, and Clinical Affairs SOPs through in-house and some on-site monitoring Conduct pre-study visits to assure the site has adequate facilities, staff, and subject population for...

OverviewAs Clinical Research Manager (CRM) in Ophthalmology, you lead clinical operations across multiple studies and countries. You will ensure compliance with ICH-GCP, SOPs, and contracts while partnering with PMs, CRAs, sponsors, and sites. This role focuses on delivering trials on time, in scope, and to high quality, within a global CRO environment. Your...

OverviewSi assicuri di inviare la sua candidatura con tutte le informazioni richieste, come indicato nella panoramica del lavoro riportata di seguito.As Clinical Research Manager (CRM) in Ophthalmology, you lead clinical operations across multiple studies and countries. You will ensure compliance with ICH-GCP, SOPs, and contracts while partnering with PMs,...

Overview In this role you coordinate the operational management of assigned clinical projects to advance Chiesi’s pipeline in line with medical standards. You act as the primary liaison to CROs, providers, and internal stakeholders, ensuring study quality, timelines, and budget adherence. You play a key part in study design input and risk management,...

Clinical Research Associate II / Senior Clinical Research (CRA) - Italy Job Category : Clinical Monitoring Requisition Number : CLINI Posted : October 1, 2026 Full-Time Remote Locations Showing 1 location Italy - RemoteDescription WhatYou'llDo: Serve as main CTI contact for assigned study sites Conduct site visits (pre-study (PSV), site initiation (SIV),...

CRA - HOMEBASED ITALY 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 Team as a Clinical Research...

As Clinical Trial Administrator, you will keep clinical trials in Italy moving with accuracy and pace. Based in Rome, you will support the local study team from start-up to close-out – managing trial documentation, tracking progress, coordinating vendors and making sure investigator sites’ payments are on time. Your work keeps trials compliant and...

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...

CRA / SENIOR CRA - Homebased (Italy) Temporary (1 year with possibility to be extended) 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...

Overview In this home-based role, you will monitor clinical trials in oncology across sites, ensuring patient safety, data integrity, and regulatory compliance. You'll work within the Strategic Resourcing Solutions team to support study conduct, site management, and quality by adhering to GCP/ICH and SOPs. You'll coordinate monitoring activities, manage...

OverviewSebbene l'esperienza professionale e le qualifiche siano fondamentali per questo ruolo, si assicuri di verificare di possedere le soft skill preferenziali, se richieste, prima di candidarsi.In this home-based role, you will monitor clinical trials in oncology across sites, ensuring patient safety, data integrity, and regulatory compliance. You'll...

BeiGene, Ltd. is seeking a Regional Clinical Trial Management Associate in Italy (remote). The role supports the Regional Clinical Study Manager in regional study delivery, oversees feasibility, start-up, document generation, and TMF tasks, and coordinates regional meetings and communications.A background in clinical research within biotech/pharma/CRO is...

Oxford Global Resources is seeking a Clinical Affairs support professional to help ensure study site selection and conduct in compliance with GCP and federal regulations.Le interessa questa opportunità? Si candidi in fretta, è previsto un elevato volume di candidature. Scorra verso il basso per leggere la descrizione completa.The role involves on-site...

If you are an experienced Senior CRA who is passionate about oncology research and looking to join a highly skilled and knowledgeable team, TRIO is the place for you!Translational Research in Oncology (TRIO)is a global clinical research organizationdedicated to advancing translational cancer research in the clinical trial setting. Our passionate team is...

Clinical Independent Rater - Romanian SpeakingControlli attentamente tutta la documentazione richiesta per la candidatura prima di fare clic sul pulsante apposito in fondo a questa descrizione.Location:Remote/VirtualHours: Estimated 10–16 hours per monthRole: Clinical Independent Rater for Clinical TrialsAbout IQVIAIQVIA is a global leader in advanced...

Clinical Independent Rater - Romanian Speaking Location: Remote/Virtual Hours: Estimated 10–16 hours per month Role: Clinical Independent Rater for Clinical Trials About IQVIA IQVIA is a global leader in advanced analytics, technology solutions, and clinical research services, dedicated to driving healthcare forward. We partner with the world’s...

Clinical Independent Rater - Romanian Speaking Location: Remote/Virtual Hours: Estimated 10–16 hours per month Role: Clinical Independent Rater for Clinical Trials About IQVIA IQVIA is a global leader in advanced analytics, technology solutions, and clinical research services, dedicated to driving healthcare forward. We partner with the world’s leading...