Senior Oncology CRA

Translational Research in Oncology (TRIO) in Italy is seeking a Senior Clinical Research Associate to join its Monitoring Resources team. This full-time, home-based role involves conducting site visits and ensuring compliance with regulations in oncology trials. Ideal candidates have substantial CRA experience, strong knowledge of medical terminology, and...

TRIO (Translational Research in Oncology) is seeking a Senior Clinical Research Associate to join our Monitoring Resources team. The role is home-based in Italy, reporting to a CRA Line Manager, with responsibilities spanning site visits, regulatory compliance, data verification, and mentoring junior CRAs. The candidate should have 5+ years CRA experience,...

Translational Research in Oncology (TRIO) in Italy is seeking a Senior Clinical Research Associate to join our Monitoring Resources team. The role is home-based in Italy and reports to a CRA Line Manager.You will conduct site visits, ensure regulatory compliance, and mentor junior CRAs. Fluency in English and a science-related Bachelor's degree are...

TR translational Research in Oncology (TRIO) is seeking a Senior Clinical Research Associate to join the Monitoring Resources team. The role is home-based in Italy, reporting to a CRA Line Manager, with responsibilities including site visits, regulatory compliance, data verification, and budget support. Requirements include 5+ years CRA experience, 2+ years...

TRIO (Translational Research in Oncology) is seeking a Senior Clinical Research Associate to join our Monitoring Resources team. The role is home-based in Italy, reporting to a CRA Line Manager, with responsibilities spanning site visits, regulatory compliance, data verification, and mentoring junior CRAs. The candidate should have 5+ years CRA experience,...

Translational Research in Oncology (TRIO) is seeking a Senior Clinical Research Associate to join the Monitoring Resources team. This home-based role in Italy requires extensive oncology trial monitoring experience and strong ICH-GCP knowledge.You will conduct site visits, ensure regulatory compliance, and mentor junior CRAs while supporting data validation...

Trial Form Support is seeking a remote Clinical Trial Monitor specializing in oncology to oversee site monitoring, data integrity, and regulatory compliance across global sites. You will ensure patient safety, validate informed consent, and manage trial documentation in line with GCP/ICH standards. In this home-based role, you will coordinate monitoring...

Syneos Health is seeking a Sponsor Dedicated CRA II/Sr CRA I/II for a home-based role in ITA. You will monitor sites, ensure GCP compliance, and support clinical studies across phases, with flexible arrangements for remote work. The ideal candidate has at least 2.5 years as a Certified CRA, oncology/Phase I experience preferred, strong communication and data...

TFS HealthScience seeks a Clinical Research Associate (CRA) to join our team as a home-based professional in Italy. You will monitor sites, ensure subject safety and data integrity, and ensure compliance with GCP/ICH guidelines. The role requires familiarity with regulatory processes and strong collaboration with project teams. The position offers a...