Clinical Research Associate I
Salva questo lavoro e mantieni la tua ricerca organizzata
Crea un account gratuito per salvare lavori, creare avvisi e tornare a questa inserzione dalla tua dashboard.
Clinical Research Associate I (CRA I) – Italy
Location: Italy
Working arrangement: Home-based with travel to clinical trial sites
Employment type: Full-time, permanent
The Opportunity
We are partnering with an international clinical research organisation seeking a Clinical Research Associate I to support clinical trials across Italy.
This opportunity would suit an early-career CRA who has gained initial clinical research or monitoring experience and is now looking to develop their independent site-management capabilities within an international CRO environment.
Key Responsibilities
- Conduct site qualification, initiation, routine monitoring and close-out visits.
- Monitor assigned clinical trial sites in accordance with study protocols, ICH-GCP and applicable Italian and European regulations.
- Review source documentation and verify the accuracy and completeness of clinical trial data.
- Ensure investigator site files and essential study documentation remain complete, accurate and inspection-ready.
- Support investigative sites with patient recruitment, data entry and query resolution.
- Identify and escalate protocol deviations, compliance concerns and site-level risks.
- Prepare accurate monitoring visit reports and follow up on outstanding actions.
- Build effective relationships with investigators, study coordinators and other site personnel.
- Collaborate with Clinical Trial Managers and wider international project teams.
- Ensure assigned sites meet agreed quality standards, recruitment objectives and study timelines.
Candidate Requirements
- Previous experience within clinical research, ideally including exposure to clinical site monitoring.
- Experience as a Junior CRA, CRA I, In-House CRA, Clinical Trial Assistant or in a similar clinical research position.
- A good understanding of clinical trial processes and ICH-GCP requirements.
- A degree in life sciences, pharmacy, nursing, medicine or another relevant discipline.
- Fluent Italian and strong professional English.
- Currently based in Italy.
- Willingness and ability to travel regularly to investigative sites across Italy.
- Strong organisational, communication and report-writing skills.
- Ability to manage multiple priorities and work effectively with limited supervision.
- A valid driving licence is preferred.
Why Consider This Opportunity?
- Develop your independent clinical monitoring experience.
- Support clinical trials within an international CRO environment.
- Work closely with experienced clinical operations professionals.
- Benefit from ongoing training and professional development.
- Build a long-term career within clinical research.
If you are based in Italy and would be interested in developing your career as a Clinical Research Associate, please apply or get in touch for a confidential discussion.
-
Clinical Research Associate
24 ore fa
como, lombardia, Italia Novartis Italia Tempo pienoSummary Sede: Field Force Italia Supporto alla Relocation: Questa posizione ha sede in Italia. Novartis non è in grado di offrire supporto per il trasferimento; ti invitiamo pertanto a candidarti solo se la sede è facilmente raggiungibile per te. Entra in un ruolo in cui il tuo lavoro contribuirà direttamente al progresso dell’innovazione clinica e ad...
-
Senior Clinical Research Associate
24 ore fa
como, lombardia, Italia 44 Premier Research S.r.l. Tempo pienoPremier Research is looking for a Senior Clinical Research Associate / Clinical Research Associate II to join our Clinical Monitoring, Site Management and SSU team. You will help biotech, medtech, and specialty pharma companies transform life-changing ideas and breakthrough science into new medicines, devices, and diagnostics. What we do is profoundly...
-
Senior Clinical Research Associate
24 ore fa
como, lombardia, Italia Translational Research in Oncology Tempo pienoIf 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...
-
Senior Clinical Research Associate
24 ore fa
como, lombardia, Italia ICON Strategic Solutions Tempo pienoICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.We are currently seeking a Senior Clinical Research Associate (CRA) to join our diverse and dynamic...
-
Experienced Clinical Research Associate
24 ore fa
como, lombardia, Italia Medpace Tempo pienoOur clinical activities are growing rapidly, and we are currently seeking full-time, home or office-based Clinical Research Associates to join our Clinical Monitoring team in Italy. This position will work with a team to accomplish tasks and projects that are instrumental to the company’s success. If you want an exciting career where you use your previous...
-
Clinical Research Associate
23 ore fa
como, lombardia, Italia Worldwide Tempo pienoWho we areWe'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 is built by those who take pioneering, creative approaches and implement them with quality and excellence. We are Worldwide Clinical Trials, and we are a global team...
-
como, lombardia, Italia Novartis Italia Tempo pienoNovartis Italia cerca un Clinical Research Associate per monitorare centri di sperimentazione clinica Fase I-IV. Sarai in contatto diretto con i centri, garantirai conformità ai protocolli, gestirai visit di avvio e fornirai formazione continua su protocolli ed emendamenti.È richiesta laurea nelle discipline scientifiche, almeno 1 anno di esperienza in...
-
Clinical Research Associate
24 ore fa
como, lombardia, Italia Worldwide Clinical Trials Tempo pienoWho 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 is built by those who take pioneering, creative approaches and implement them with quality and excellence. Who We Are We’re a global, midsize CRO that pushes...
-
Clinical Research Associate
24 ore fa
como, lombardia, Italia Parexel Tempo pienoParexel 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...
-
como, lombardia, Italia IQVIA LLC Tempo pienoClinical 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...
