Offerte di lavoro per ich in Firenze

Responsibilities (a) Site management Study site selection, initiation (SIV) and clinical monitoring. Perform pre-study visit to ensure eligible sites are selected according to sponsor site selection criteria, including but not limited to adequate resources and experience. Prepare and conduct SIV to ensure adequate study training for relevant site...

Fb Industry Automation entwickelt und realisiert maßgeschneiderte Gesamtlösungen für die Intralogistik. Als Systemintegrator verbinden wir unterschiedliche Technologien zu Lösungen, die auf die Prozesse und Anforderungen unserer Kunden abgestimmt sind. Um unsere Präsenz in Italien weiter auszubauen, suchen wir einen selbstständigen Vertriebspartner,...

PQE Group, una società di consulenza leader mondiale nell'industria farmaceutica e dei Medical Device, cerca un QA professional per supportare Process & Cleaning Validation in Toscana. Sede: Reggello (FI).Attività internazionali e trasferimenti presso i clienti con viaggio medio del 50%. Si richiede Laurea in discipline scientifiche, almeno 3 anni di...

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...

TFS HealthScience is seeking a Freelance Senior Clinical Research Associate (0.4 FTE) to support ophthalmology studies from home in Italy. The role involves on-site or remote monitoring, protocol compliance, and collaboration with sponsors and study teams.The ideal candidate will have 5+ years of independent monitoring experience, GCP/ICH knowledge, and...

IQVIA is seeking an Experienced Clinical Research Associate, Site to perform monitoring and site management duties needed to ensure studies are conducted according to protocol, GCP, ICH guidelines, and sponsor requirements. You will conduct site visits—from selection to close-out—and ensure timely data reporting and regulatory compliance.The role...

IQVIA seeks an Experienced Clinical Research Associate to work from home in Italy. You will perform site monitoring and site management to ensure studies are conducted per protocol, GCP, and ICH guidelines.You will coordinate monitoring visits and ensure timely data reporting to sponsors in a fully remote role. The position emphasizes monitoring activities,...

Chiesi in Parma seeks a senior leader to drive industrialization and lifecycle management of upstream biopharmaceutical processes. You will lead insourcing, tech transfer, scale‑up, and validation across development to commercial production.The role interfaces with R&D, CDMOs, Production, Quality, and Engineering, applying QbD and ensuring alignment with...

Worldwide Clinical Trials is seeking a Clinical Operations Site Manager/CRA leadership role in Rome, Italy. You will interview, select, and onboard CRA/IHCRA candidates and ensure timely training for site visits. You will mentor CRAs on-site, review quality metrics, and escalate performance issues as needed. Travel is required; strong knowledge of FDA...

IQVIA is seeking an Experienced Clinical Research Associate, Site to perform monitoring and site management duties needed to ensure studies are conducted according to protocol, GCP, ICH guidelines, and sponsor requirements. You will conduct site visits—from selection to close-out—and ensure timely data reporting and regulatory compliance.Scopra...

Worldwide Clinical Trials is seeking a Clinical Operations Site Manager/CRA leadership role in Rome, Italy. You will interview, select, and onboard CRA/IHCRA candidates and ensure timely training for site visits. You will mentor CRAs on-site, review quality metrics, and escalate performance issues as needed. xbvzest Scorra verso il basso per una panoramica...

Chiesi Farmaceutici S.p.A. seeks a Clinical Project Manager for Global Rare Diseases to coordinate operational management of assigned trials in line with ICH GCP and Chiesi SOPs.Candidarsi per questo ruolo è semplice. Scorra verso il basso e faccia clic su "Candidati" per essere preso/a in considerazione per questa posizione.This permanent, remote-friendly...

Translational Research in Oncology (TRIO) is seeking a Clinical Research Associate to join the Monitoring Resources team in a home-based role in Italy. The ideal candidate will have at least 2 years of monitoring experience specifically in oncology trials and must be fluent in English. Responsibilities include conducting site visits and ensuring compliance...

IQVIA seeks an Experienced Clinical Research Associate to work from home in Italy. You will perform site monitoring and site management to ensure studies are conducted per protocol, GCP, and ICH guidelines.Si assicuri che tutte le informazioni della sua candidatura siano aggiornate e corrette prima di cogliere questa opportunità.You will coordinate...

Sei pronto per entrare a far parte di una società di consulenza leader mondiale nell'industria farmaceutica e dei Medical Device? PQE Group è affermata in questo settore dal 1998, garantendo una presenza internazionale grazie alle 45 filiali e i 2000 dipendenti in Europa, Asia e nelle Americhe. Lavorare in una realtà di consulenza come PQE Group ti...

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: R Job Overview Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting...

Are you an experienced Clinical Research Associate looking to join a dynamic and growing clinical research organisation? We are seeking a CRA II to manage investigative sites across Italy, ensuring clinical trials are conducted in accordance with study protocols, ICH-GCP, and applicable regulatory requirements. Key Responsibilities Conduct site...

Senior ML Engineer – Production Systems (m/w/d) In unbefristeter Festanstellung. Gehalt: nach Berufserfahrung. Remote. Ref. 30865 Mein Mandant entwickelt eine innovative Softwareplattform, die die operative Planung in Werkstätten nachhaltig effizienter und transparenter macht. Die Plattform wird täglich in hunderten Betrieben produktiv eingesetzt und...

PQE Group, una società di consulenza leader mondiale nell'industria farmaceutica e dei Medical Device, cerca un QA professional per supportare Process & Cleaning Validation in Toscana. Sede: Reggello (FI).Attività internazionali e trasferimenti presso i clienti con viaggio medio del 50%. Si richiede Laurea in discipline scientifiche, almeno 3 anni di...

Parexel FSP is hiring for two experienced CRA's at either the CRA II or Senior CRA level to join one of a large Sponsor’s in the EU.This role is responsible for the site management, site monitoring and close-out of assigned clinical trials investigator sites to ensure patient safety and quality study executionSome Specifics About This Advertised RoleEnsure...