Adecco per importante azienda cliente del settore farmaceutico veterinario, ricerca un/unaSenior Regulatory Affairs. Responsabilità principali Gestione completa dei dossier regolatori (CESP, UPD): redazione, aggiornamento e mantenimento delle AIC. Coordinamento delle attività di registrazione, variazioni e submission verso le autorità competenti. Interazione con Ministero della Salute, EMA e...
Talent Solutions, part of Manpower Group, for an important pharmaceutical client based in Florence, is currently recruiting for a Regulatory Affairs Central and Latin America Coordinator Are you a highly motivated and detail-oriented regulatory professional looking to make a significant impact on a global scale? Do you thrive in a fast-paced environment where your expertise directly contributes...
Randstad Talent Selection Hopportunities è la specialty che si occupa di Ricerca & Selezione di professionisti qualificati appartenenti alle categorie protette. Il nostro cliente è un'importante realtà internazionale e ci ha incaricato di ricercare la figura di Regulatory Affairs Administration Assistant_legge ***** (invalidità civile) Si offre un contratto full time a tempo tempo determinato di...
Talent Solutions, part of Manpower Group, for an important pharmaceutical client based in Florence, is currently recruiting for a Global Regulatory Affairs Operations Innovation and Information Management Senior Associate The resource will join the Global Regulatory Affairs Operations department as a Senior Associate in the Innovation and Information Management (IIM) area. Reporting to the IIM...
Ruolo: Senior Clinical Affairs Luogo: posizione full remote ALTEN supporta le strategie di sviluppo dei propri clienti nelle aree dell’innovazione, della R&D e dei sistemi informativi tecnologici. Nato più di 30 anni fa e presente in 30 Paesi, il Gruppo ALTEN si è affermato come leader mondiale nell’ingegneria e nei Servizi IT e leader Europeo per la consulenza nell'industria Life...
Overview POSITION SUMMARY: The Senior Clinical Research Associate (Senior CRA) is responsible for scheduling and conducting on-site and remote monitoring visits in compliance with applicable regulatory standards (MDR, ISO 14155, ICH/GCP guidelines, Teleflex procedures and IRB/EC policies and procedures). The Senior CRA conducts monitoring visits as identified by the monitoring plan, study team...
POSITION SUMMARY : The Senior Clinical Research Associate (Senior CRA) is responsible for scheduling and conducting on-site and remote monitoring visits in compliance with applicable regulatory standards (MDR, ISO *****, ICH/GCP guidelines, Teleflex procedures and IRB/EC policies and procedures). The Senior CRA conducts monitoring visits as identified by the monitoring plan, study team or...
Senior Clinical Research Associate (Oncology) Working embedded with a leading global oncology-focused biopharmaceutical company We are partnering with a top-tier global biopharmaceutical organisation to support a growing oncology portfolio and are seeking an experienced Clinical Research Associate to join the team in an advanced, hands-on clinical role. This position offers the opportunity to...
Senior Clinical Research Associate – Remote (Italy) | €50,000 - €65,000 + Car Allowance Ready to take the next step in your CRA career? This is your chance to join a leading global organization that prioritizes your development and success. You’ll work remotely with approximately 6–8 site visits per month across Italy, gaining exposure to diverse protocols and therapeutic areas - including...
Precision for Medicine is not your typical CRO. We are passionate about cultivating our culture and are proud to share extremely high CRA retention rates compared to industry averages. CRAs join us, love their jobs, and stay because of the amazing people and enjoyable quality of life. You will focus on an average of one to two studies setting you up to be a protocol expert. Travel is reasonable...
Upsilon Global are seeking a freelance CRA based in Italy to perform remote monitoring visits and site management activities across 5 sites for a cardiology study. This is estimated to be 0.5 FTE, starting in October and working with an expanding CRO with operations across US, EU and APAC regions. Regulatory and start-up activities have been performed and we now need a local expert to take over...
Veeda Lifesciences is seeking a Clinical Research Associate (CRA) based in Italy for its growing international hematology/oncology Clinical Trials program. This is a full-time job. Job overview: The CRA is responsible for ensuring that the conduct of a clinical trial at selected Investigational Sites is according to the currently approved protocol/amendments, ICH GCP guidelines, the applicable...
Your new company Our client is a leading company in the Pharma Sector. We are seeking a Senior Clinical Research Associate to join our team You new role - Ensure compliance with client SOPs, study protocols, ICH-GCP and applicable regulations - Train and support investigator site teams on study procedures and systems - Conduct site initiation, monitoring (on-site and remote), and close‑out...
Our client is a leading company in the Pharma Sector. We are seeking a Senior Clinical Research Associate to join our team You new role - Ensure compliance with client SOPs, study protocols, ICH-GCP and applicable regulations - Train and support investigator site teams on study procedures and systems - Conduct site initiation, monitoring (on-site and remote), and close‑out visits - Verify...
Get AI-powered advice on this job and more exclusive features. Team Manager - ITC Recruitment Hays Italia Your new company Our client is a leading company in the Pharma Sector. We are seeking a Senior Clinical Research Associate to join our team Your new role - Ensure compliance with client SOPs, study protocols, ICH-GCP and applicable regulations - Train and support investigator site teams...
Per nostro cliente, leader del settore farmaceutico, stiamo ricercando un/a Assistente Amministrativo con Inglese fluente - appartenente alle categorie protette (Art. 1 L*****) Inserita all'interno del dipartimento Global Regulatory Affairs Operations, la risorsa ricercata sar caratterizzata da una naturale propensione a rispettare le scadenze, a gestire i processi con rigore ed a mantenere un...
Your new company Our client is a leading company in the Pharma Sector. We are seeking a Senior Clinical Research Associate to join our team You new role Ensure compliance with client SOPs, study protocols, ICH-GCP and applicable regulations Train and support investigator site teams on study procedures and systems Conduct site initiation, monitoring (on-site and remote), and close-out...
A leading medical device company in Tuscany is seeking a Senior Clinical Research Associate to conduct monitoring visits and ensure compliance with regulatory standards. The ideal candidate will have at least 5 years of clinical trial monitoring experience, strong communication skills, and the ability to work independently. Proficiency in both Italian and English is required. This role involves...