Stipendio medio: euro48.586 /annuale
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- A leading clinical research organization in Milan is seeking a CRA II - III to oversee clinical trials. This position requires a university degree in life sciences, at least 2-3 years of clinical trial monitoring experience, and a strong knowledge of ICH GCP Guidelines...ConsigliatoLavoro da casaOrario flessibile
- ...the trust of new customers and secure continued growth of the company. We’re expanding our team in Italy and looking for a new CRA (CRA II - III, depending on experience) . Whether you’re building your expertise as a CRA I or ready to step into a higher CRA role, this...ConsigliatoLavoro da casaOrario flessibile
- ...diverse soft skill ed esperienze. La preghiamo di consultare attentamente la panoramica riportata di seguito. Sponsor Dedicated CRA II - Home Based ITA Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer...ConsigliatoLavoro da casaRemoto
- ...CRA - multi-sponsor ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an... ...and close-out investigational sites for clinical studies in phases II – IV, ensuring adherence to applicable regulations and principles...ConsigliatoImpiego permanenteContratto con partita IVAOrario flessibile
- ...CRA II / Senior CRA ICON 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...ConsigliatoImpiego permanenteContratto con partita IVAOrario flessibile
- ...mission to shape the future of clinical development. As a Senior CRA / Clinical Site Manager you will be joining the world’s largest &... .... Responsibilities You will monitor multiple Phase I, II, III & IV clinical trial sites You will utilise your customer...ConsigliatoContratto con partita IVARemotoOrario flessibile
- ...If you are an experienced 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 organization dedicated to advancing...ConsigliatoOrario flessibile
125000 $ - 145000 $
...: be courageous, be accountable, be honest, be inclusive and elevate others.**Job Description Summary****Job Description**## ROLEThe CRA is an important member of the Alira Health Clinical team. The CRA is highly motivated and functions independently to conduct site monitoring...ConsigliatoRemotoOrario flessibile125000 $ - 145000 $
A global healthcare consulting firm is seeking a Clinical Research Associate (CRA) to monitor clinical trials, ensuring compliance with guidelines and quality standards. The CRA will collaborate with various teams to address site questions, assist in recruitment, and ensure...ConsigliatoRemoto- A global clinical research organization in Tuscany is seeking an experienced Clinical Research Associate to join their Monitoring Resources team. The role involves conducting site visits, ensuring regulatory compliance, and mentoring junior team members. Candidates should...ConsigliatoRemotoOrario flessibile
- A global biopharmaceutical company in Italy seeks a Senior Clinical Research Associate to execute clinical monitoring activities according to ICH guidelines and GCP regulations. The role involves managing sites for oncology clinical trials, ensuring compliance, and mentoring...ConsigliatoRemoto
- A leading clinical research organization in Milan is seeking a Clinical Site Manager to oversee multiple clinical trials in Oncology. The ideal candidate will have a Bachelor's degree and over 4 years of relevant experience. Responsibilities include monitoring clinical ...Consigliato
- ...future. This is a great opportunity for experienced Senior CRA's currently working within the life science sector for pharmaceutical... ...independent monitoring experience in clinical development phases II-IV Understanding of ICH-GCP, EU and FDA requirements...ConsigliatoLavoro da remotoTempo pienoDisponibilità immediataOrario flessibile
- ...Certification in compliance with Ministerial Decree of 15 November 2011 (Official Gazette no. 11 of 14/01/2021). Experience as a CRA and/or Study Coordinator in clinical trials. Previous experience in the field oncology and onco-haematology, but not limited to this...ConsigliatoDisponibilità immediataLavoro ibridoRemoto
- ...highly motivated, collaborative, and most importantly, share our passionate interest in fighting cancer.**General Description:*** The CRA executes clinical monitoring activities at clinical trial sites and monitors clinical trials in accordance with ICH guidelines and...Consigliato
- CRA II / Senior CRA ICON Biotech ICON 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...Impiego permanenteContratto con partita IVAOrario flessibile
- ...Qualifications: University Bachelor's Degree and Master's Degree in scientific discipline or health care In possession of CRA Certification as required by Ministerial Decree dated 15.11.2011 Experience in Pharma Industry, and/or Clinical Trials environment...Tempo pienoOrario flessibile
- ...and supporting research activities to achieve project objectives. ~ ONLY CV WITH DM 15/11/11 CERTIFICATION AND PROVEN EXPERIENCE AS CRA (MINIMUM 3 VISIT IN AUTONOMY ) WILL BE TAKEN INTO CONSIDERATION. Qualifications Proficiency in Clinical Research Associates'...Tempo pienoLavoro ibrido
- ...applicable regulations. Evaluate the quality and integrity of study site, performing periodical reviews (TMF and TCF) Support CPM and CRA on the development and maintenance of Trial Master File and Trial Center Files Assist the CPM, tracking regulatory submissions and...Stage/Tirocinio
- A global clinical research organization is seeking an experienced Clinical Research Associate to join their Monitoring Resources team. The role involves conducting site visits, ensuring compliance with regulations, and mentoring junior staff. Candidates should have at least...RemotoOrario flessibile
- A global biotechnology company is seeking a Clinical Research Associate in Italy to execute clinical monitoring activities in oncology and hematology trials. The role involves collaborating with clinical operations, ensuring compliance with regulations, and maintaining ...Remoto
- A leading biomedical research company in Milano is seeking a Clinical Research Associate to manage clinical trials within a multidisciplinary team. This hybrid role combines remote work with office presence and requires at least 2 years of experience, knowledge of GCP guidelines...Lavoro ibridoRemoto
- ...requirement.Qualifications* University Bachelor's Degree and Master's Degree in scientific discipline or health care* In possession of CRA Certification as required by Ministerial Decree dated 15.11.2011* Experience in Pharma Industry, and/or Clinical Trials environment*...Lavoro da casa
- A global clinical research organization is seeking an experienced Clinical Research Associate to join their Monitoring Resources team in a home-based position in Italy. The ideal candidate will have a minimum of 2 years of monitoring experience in oncology trials and strong...RemotoOrario flessibile
- ...In-House CRA ICON 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...Impiego permanenteContratto con partita IVALavoro ibridoOrario flessibile
- ...Trentino-Alto Adige e Friuli-Venezia Giulia) Posizione: Ausiliaria/o addetta alle pulizie per inserimento presso nostra CRA (casa di riposo per anziani non autosufficienti) situata ad Ancarano di Rivergaro (Provincia di Piacenza) Le risorse individuate...Impiego permanentePart-timeTurniWeekend
- ...in scientific discipline or health care • Requires at least 3 years of year of on-site monitoring experience • In possession of CRA Certification according to Ministerial Decree dated 15.11.2011 • Good knowledge of, and skill in applying, applicable clinical...Tempo pieno
- ...benessere lavorativo e progetti di welfare per supportare il work-life balance. Posizione: Si ricerca Ausiliario/a per CRA di Guastalla Requisiti: Le risorsa individuata darà supporto alle attività di base, e trasporto anziani ·Essere automuniti...Impiego permanente
- A leading clinical research organization in Italy is seeking a Clinical Site Manager. Massimizzi le sue possibilità di successo assicurandosi che il suo CV e le sue competenze corrispondano ai requisiti di questa posizione. The successful candidate will monitor multiple...
- Select how often (in days) to receive an alert: Laboratory Analyst Date: Jan 9, 2026 City : Ravenna, Emilia-Romagna, Italy State : Emilia-Romagna (IT-45) Country : Italy (IT) Requisition Number: 43244 We are seeking a Laboratory Analyst to join our team...TurniOrario flessibileWeekend


