Freelance Clinical Research Associate
3 settimane fa
We are looking for a Part-Time Freelance CRA to strengthen our clinical operations in Italy. Preference will be given to candidates based in or around Rome, Pisa, Livorno, Grosseto, or Florence. Job Requirements: Bachelor’s degree required – preferred qualification in life sciences or medical sciences Minimum 3 years of experience of onsite monitoring activities Previous experience in Cardiovascular Disease research Profound knowledge of clinical research processes and medical terminology Expert knowledge of ICH GCP, and international and local regulatory requirements Passion for clinical research English language proficiency of minimum level C1 (ref. CEFR) – fluent in written and spoken English Driving license B and ability to travel Job Responsibilities: You would be primarily responsible for monitoring clinical trials and Ensuring that clinical trial is conducted, recorded, and reported in accordance with all applicable international and local regulations and guidelines, good practices, SOPs and Clinical Trial Protocol Ensuring data quality and integrity meet acceptable clinical standards Guaranteeing the rights and safety of patients involved in a study are protected Performing and coordinating all aspects of the clinical monitoring and site management process Conducting remote and on-site visits to assess protocol and regulatory compliance and managing required documentation Developing collaborative relationships with investigational sites, act as a site processes specialist, ensuring that the trial is conducted in accordance with the approved protocol, ICH-GCP guidelines, applicable regulations, and SOPs to guarantee subjects rights, well-being, and data reliability; and you would ensure audit readiness. Serving as facilitator of Clinical Trial conduct in respective area in terms of identifying qualified sites and investigators, facilitating communication between sponsor and regulatory authorities and trial sites. What We Offer: Competitive Pay – Fair compensation based on skills and experience. Friendly environment – in a privately owned international company. Mentorship and Guidance – Support from senior team members to enhance learning. You can apply via the link or send a CV directly to: careers@sanaclis.com *SanaClis is an equal opportunity and inclusive employer
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Freelance clinical research associate
4 settimane fa
Rome, Italia SanaClis A tempo pienoWe Are Hiring! We are looking for a Part-Time Freelance CRA to strengthen our clinical operations in Italy. Preference will be given to candidates based in or around Rome, Pisa, Livorno, Grosseto , or Florence . Job Requirements: Bachelor’s degree required – preferred qualification in life sciences or medical sciences Minimum 3...
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Freelance Clinical Research Associate
4 settimane fa
Greater Rome Metropolitan Area, Italia SanaClis A tempo pienoWe Are Hiring! We are looking for a Part-Time Freelance CRA to strengthen our clinical operations in Italy. Preference will be given to candidates based in or around Rome, Pisa, Livorno, Grosseto , or Florence . Job Requirements: Bachelor’s degree required – preferred qualification in life sciences or medical sciences Minimum 3 years of experience of...
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Freelance Clinical Research Associate
4 settimane fa
Greater Rome Metropolitan Area, Italia SanaClis A tempo pienoWe Are Hiring!We are looking for a Part-Time Freelance CRA to strengthen our clinical operations in Italy. Preference will be given to candidates based in or around Rome, Pisa, Livorno, Grosseto, or Florence.Job Requirements:Bachelor’s degree required – preferred qualification in life sciences or medical sciencesMinimum 3 years of experience of onsite...
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Clinical trial monitoring associate
4 settimane fa
Rome, Italia Nouscom A tempo pienoNouscom is a private clinical stage immuno-oncology company developing next-generation, off-the-shelf and personalized cancer vaccines. Our proprietary viral vector platform has the capacity to encode for large payloads of neoantigens or other immunomodulators and is clinically demonstrated to safely and potently harness the power of the immune system.We are...
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Clinical Trial Monitoring Associate
3 settimane fa
Rome, Italia Nouscom A tempo pienoNouscom is a private clinical stage immuno-oncology company developing next-generation, off-the-shelf and personalized cancer vaccines. Our proprietary viral vector platform has the capacity to encode for large payloads of neoantigens or other immunomodulators and is clinically demonstrated to safely and potently harness the power of the immune system.We are...
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Clinical Trial Monitoring Associate
4 settimane fa
Rome, Italia Nouscom A tempo pienoNouscom is a private clinical stage immuno-oncology company developing next-generation, off-the-shelf and personalized cancer vaccines. Our proprietary viral vector platform has the capacity to encode for large payloads of neoantigens or other immunomodulators and is clinically demonstrated to safely and potently harness the power of the immune system. We...
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Clinical Trial Monitoring Associate
3 settimane fa
Greater Rome Metropolitan Area, IT Nouscom A tempo pienoNouscom is a private clinical stage immuno-oncology company developing next-generation, off-the-shelf and personalized cancer vaccines. Our proprietary viral vector platform has the capacity to encode for large payloads of neoantigens or other immunomodulators and is clinically demonstrated to safely and potently harness the power of the immune system. We...
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Clinical Quality Assurance Manager
4 settimane fa
Rome, Italia Adecco A tempo pienoAdecco Italia Spa_Life Science is looking for a “Clinical Quality Assurance Manager”in preparation for the expansion of clinical activities, plans to strengthen the office of clinical quality assurance. The position will be responsible to assess compliance with SOPs, GxP, European regulations, local regulations and guidelines, and clinical study...
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Clinical Research Associate
4 settimane fa
Rome, Italia EPM Scientific A tempo pienoCerchiamo un CRA Junior, in Italia, motivato per supportare studi clinici garantendo qualità e conformità. Requisiti: - 1-3 anni di esperienza come CRA (ruolo Junior). - Esperienza in visite pre-site. - Ottima conoscenza delle lingue inglese e italiano. - Capacità di lavorare in modo indipendente e in team. - Eccellenti capacità comunicative e...
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Cra/scra. home based
4 settimane fa
Rome, Italia Pivotal A tempo pienoPivotal is excited to expand our team and we are looking for an experienced, highly motivated Clinical Research Associate who shares our vision of providing clinical research excellence.Joining Pivotal as a CRA/SCRA means that you’ll enjoy being a member of one of the leading full-service contract research organizations in Europe with a very solid...
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Junior Statistical Sas Programmer
4 settimane fa
Rome, Italia OPIS A tempo pienoThe Junior Statistical SAS Programmer, under the supervision of the Direct Manager, is mainly involved in developing SAS programs for the generation of datasets, tables, figures and listings for clinical studies (according to ICH E3), publications or Health Authorities requests. Collaborates with Biostatistics and Data Management staff on clinical...
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Junior statistical sas programmer
4 settimane fa
Rome, Italia OPIS A tempo pienoThe Junior Statistical SAS Programmer, under the supervision of the Direct Manager, is mainly involved in developing SAS programs for the generation of datasets, tables, figures and listings for clinical studies (according to ICH E3), publications or Health Authorities requests. Collaborates with Biostatistics and Data Management staff on clinical...
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Junior Statistical SAS Programmer
3 settimane fa
Rome, Italia OPIS A tempo pienoThe Junior Statistical SAS Programmer, under the supervision of the Direct Manager, is mainly involved in developing SAS programs for the generation of datasets, tables, figures and listings for clinical studies (according to ICH E3), publications or Health Authorities requests. Collaborates with Biostatistics and Data Management staff on clinical...
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CRA/SCRA. Home based
4 settimane fa
Rome, Italia Pivotal A tempo pienoPivotal is excited to expand our team and we are looking for an experienced, highly motivated Clinical Research Associate who shares our vision of providing clinical research excellence.Joining Pivotal as a CRA/SCRA means that you’ll enjoy being a member of one of the leading full-service contract research organizations in Europe with a very solid...
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CRA/SCRA. Home based
3 settimane fa
Rome, Italia Pivotal A tempo pienoPivotal is excited to expand our team and we are looking for an experienced, highly motivated Clinical Research Associate who shares our vision of providing clinical research excellence.Joining Pivotal as a CRA/SCRA means that you’ll enjoy being a member of one of the leading full-service contract research organizations in Europe with a very solid...
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Exec Account Director, Business Development
4 settimane fa
Rome, Italia ThermoFisher A tempo pienoWork ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionAt Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed...
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Radiopharma research specialist
3 settimane fa
Rome, Italia Medipass - Ergéa Group A tempo pienoMEDIPASS IN BREVEMedipass S.p. A. è il principale fornitore di soluzioni cliniche integrate per la radioterapia, la diagnostica per immagini e la medicina nucleare in Italia.Da oltre 30 anni collaboriamo con ospedali e strutture sanitarie, pubbliche e private, per definire ed implementare la strategia migliore riguardo dotazioni tecnologiche, organizzazione...
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Freelance Regulatory Affairs Consultant
4 settimane fa
Rome, Italia Planet Pharma A tempo pienoJob SummaryProvide regulatory and technical support for assigned products, including submissions, documentation, and project-related regulatory activities.Key Responsibilities:Stay updated on local regulatory requirements, communicating changes to stakeholders.Handle inquiries on compassionate use, early access programs, labeling exemptions, and clinical...
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Freelance regulatory affairs consultant
4 settimane fa
Rome, Italia Planet Pharma A tempo pienoJob SummaryProvide regulatory and technical support for assigned products, including submissions, documentation, and project-related regulatory activities.Key Responsibilities:Stay updated on local regulatory requirements, communicating changes to stakeholders.Handle inquiries on compassionate use, early access programs, labeling exemptions, and clinical...
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Freelance Regulatory Affairs Consultant
3 settimane fa
Rome, Italia Planet Pharma A tempo pienoJob SummaryProvide regulatory and technical support for assigned products, including submissions, documentation, and project-related regulatory activities. Key Responsibilities: Stay updated on local regulatory requirements, communicating changes to stakeholders. Handle inquiries on compassionate use, early access programs, labeling exemptions, and clinical...