Senior Clinical Research Associate

CRA / SENIOR CRA - Homebased (Italy)Temporary (1 year with possibility to be extended)TFS HealthScience is a leading global mid-size Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies throughout their entire clinical development journey. Our expertise includes full service-capabilities, resourcing and...

If 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!Scorra verso il basso per trovare i dettagli completi dell'offerta, inclusa l'esperienza richiesta e le mansioni associate.Translational Research in Oncology (TRIO)is a global clinical research...

OverviewIn this home-based role, you will monitor clinical trials in oncology across sites, ensuring patient safety, data integrity, and regulatory compliance. You’ll work within the Strategic Resourcing Solutions team to support study conduct, site management, and quality by adhering to GCP/ICH and SOPs. You’ll coordinate monitoring activities, manage...

If 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!Le interessa questa opportunità? Si candidi in fretta, è previsto un elevato volume di candidature. Scorra verso il basso per leggere la descrizione completa.Translational Research in Oncology...

If 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...

CTI is seeking a Clinical Research Associate II / Senior CRA to support sites in Italy, focusing on regulatory compliance and timely deliverables. You will act as the main CTI contact for assigned sites and manage site visits throughout pre-study through close-out phases.The role requires 3–5 years of CRA experience with a strong life-science background,...

Trial Form Support is seeking a remote oncology clinical monitors to oversee trials across sites, ensuring patient safety, data integrity and regulatory compliance in a fast-paced setting.The role supports study conduct, site management and quality with GCP/ICH adherence, coordinating monitoring activities and audits while enabling meaningful patient...

Trial Form Support is seeking a remote Monitoring Specialist to oversee oncology clinical trials across sites, ensuring patient safety, data integrity, and regulatory compliance per GCP/ICH and SOPs.Possiede le competenze per ricoprire questo ruolo? Legga i dettagli completi qui sotto e invii la sua candidatura oggi stesso.Based in a globally collaborative...

Provide support to Clinical Affairs team to assure study site selection and conduct of the study by study sites in compliance with Good Clinical Practices, federal regulations, and Clinical Affairs SOPs through in-house and some on-site monitoringConduct pre-study visits to assure the site has adequate facilities, staff, and subject population for conducting...