Stipendio medio: euro60.000 /annuale
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- ...programs, medical education, and healthcare communication. We’re currently looking for a proactive Clinical Research Associate (CRA) to join our Clinical Operations team in a hybrid role (Milan-based) . What you’ll do Ensure studies are conducted in compliance...ConsigliatoLavoro ibrido
- The Sr CRA is an important member of the Alira Health Clinical team. The Sr CRA is highly motivated and functions independently to conduct... ...: 3 years of experience in the pharmaceutical / biotechnology / CRO industry, 2 year of clinical monitoring experience with 1 year of...ConsigliatoRemotoOrario flessibile
- ...Antares Consulting SA is looking to hire a proactive Clinical Research Associate (CRA) to join our Clinical Operations team in a hybrid role based in Milan. The CRA will be responsible for ensuring compliance with clinical protocols and regulations while performing site...ConsigliatoLavoro ibrido
- ...seeking a Senior Clinical Research Associate to join the Monitoring Resources team. The role is home-based in Italy, requiring 5 years of CRA experience and 2 years in oncology trials. Responsibilities include site visits, ensuring regulatory compliance, and mentoring junior...ConsigliatoRemotoOrario flessibile
- Parexel International is looking to hire several Clinical Research Associates II in Italy. Candidates must have at least 2 years of independent monitoring experience in a similar setting. The role involves managing site quality, building relationships with site staff, ...Consigliato
- ...study progress, and ensuring adherence to regulatory requirements. Candidates should hold a Master's Degree in Life Sciences and have CRA certification. Strong communication and organizational skills, along with some experience in clinical research, are crucial. The...ConsigliatoTempo pieno
- 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...ConsigliatoRemotoOrario flessibile
- ...Todayjob requisition id: JR101971**Who we are**We’re a global, midsize CRO that pushes boundaries, innovates and invents because the path to... ...on the lives of patients. As a Clinical Research Associate (CRA) at Worldwide, you will find yourself working alongside brilliant...ConsigliatoStage/TirocinioRemoto
1.947 €/mese
Nuova vita cooperativa sociale a Cesena cerca un/una Coordinatore/Coordinatrice per Casa Residenza Anziani. Il candidato ideale deve avere almeno 2 anni di esperienza nel ruolo e possedere un diploma o laurea in Servizio sociale o campi affini. Offriamo un contratto...ConsigliatoImpiego permanente- Parexel International is seeking to hire Clinical Research Associate II positions to join their team in Italy. Candidates should have at least 2 years of independent monitoring experience. The role involves managing clinical sites, ensuring compliance with regulations,...Consigliato
1.947 €/mese
...promuovere la crescita professionale delle persone. Requisiti Esperienza: almeno 2 anni nel ruolo di Coordinatore/Coordinatrice in CRA (obbligatorio). Titoli di laurea o diplomi ammessi (almeno triennale, ai fini dell’accesso dall’esterno, come da normativa vigente...ConsigliatoImpiego permanenteTempo pienoTurniDal lunedì al venerdì- ...communities depend on – now and in the future. This is a great opportunity for CRA's currently working within the life science sector for pharmaceutical companies, biotech companies or CRO's to work with a world-leading CRO across multiple sponsors, various protocols...ConsigliatoLavoro da remotoTempo pienoDisponibilità immediataOrario 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
- ...Parexel is pleased to announce we are looking to hire several CRA II for the team in Italy. Candidates must have close to atleast 2 years independent monitoring experience in a similar setting. The role can be based in any major Italian city as strong transport links are...ConsigliatoDisponibilità immediataRemotoOrario flessibile
- ...inventory, dispensing, dosing, and disposition requirements. EU CRAs could have a shared role of Regulatory Affairs Officer (RAO) and CRA. The Regulatory department will oversee the RAO role while the Clinical Operations Manager (COM) will oversee the CRA role. Duties...Consigliato
- ...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
- ...site management in Milan, Italy. The role is home-based and requires a Bachelor's and Master's degree in relevant fields, along with CRA certification. Applicants should have strong computer skills, excellent English command, and the ability to build effective relationships...Lavoro da casa
- ...Job Summary Medpace is the leading CRO for Biotech companies and is continuing to add Clinical Trial Managers of different experience levels to join our Clinical Trial Management Group in our Milan office. Clinical Trial Managers with expertise in Immunology and Infectious...RemotoOrario flessibile
- 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
- ...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 development...Contratto con partita IVAOrario flessibile
- ...agreement and retrieve invoices according to local requirement.Qualifications • Master's Degree in Life Sciences.• In possession of CRA certification according to Ministerial requirements. • Completion of CRA training program or prior monitoring experience. • Basic knowledge...Disponibilità immediata
- ...processes, and ensuring compliance with regulatory requirements. Candidates should have a 4-year degree or RN/BSN in Nursing with at least 2 years of CRA experience. Strong communication, organizational skills, and proficiency in relevant tools are required. #J-18808-Ljbffr...Remoto
- 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
- ...–6 years of clinical trial experience within pharma, biotech, or CRO environments ~ Hands on experience managing complex global interventional... ...gained through a combination of site level roles (e.g. CRA) and clinical study management responsibilities ~ Demonstrated...
- ...Principal Investigators (PIs) and site teams, supports study start‑up and recruitment, and provides in‑field oversight of CRO activities—particularly CRA performance—as part of Recordati’s Sponsor oversight responsibilities. The CTLM serves as a key escalation point for...Part-timeTempo pienoRemoto
- A leading clinical research organization in Lombardia, Italy, is seeking a Clinical Research Associate to oversee the initiation, monitoring, and closing of clinical trial sites. Responsibilities include ensuring compliance with regulations and GCPs, conducting monitoring...
- ICON, a leading healthcare intelligence and clinical research organization, is seeking a Senior Clinical Research Associate (CRA) in Rome, Lazio. This role involves overseeing clinical trial activities to ensure adherence to protocols and regulatory requirements. The ideal...Orario flessibile
- ...management for clinical studies according to Fortrea, and/or Sponsor, Standard Operating Procedures, and Regulatory Guidelines. The Sr CRA assures the implementation of project plans as assigned, functions as leader for projects of limited scope, as assigned and assumes...Impiego permanente
- ...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 development...Impiego permanenteContratto con partita IVAOrario flessibile
- ...CRA I - 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 of clinical...Impiego permanenteContratto con partita IVAOrario flessibile
