21 ago - Cuneo
Altro
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 organization dedicated to advancing translational cancer research in the clinical trial setting. TRIO is looking for a Senior Clinical Research Associate to join our Monitoring Resources team. Reporting to a CRA Line Manager, this position will be home-based in Italy. This is a full-time position.
Responsibilities Conducting site visits, including pre-study, initiation, monitoring, and termination
- Confirming adherence to all FDA, ICH-GCP and local regulations
- Ensuring the completion and collection of regulatory documents
- Performing data verification of source documents
- Ensuring implementation and compliance with FDA, ICH-GCP guidelines
- Participating in budget negotiation and follow-up where applicable
- Assisting with data validation and query resolution; xrdztoy Qualifications A minimum of 2 years of monitoring experience in oncology trials Minimum 5 years of previous CRA experience Experience in monitoring early-phase trials Read, write and speak fluent English Completion of a science-related Bachelor's degree Excellent knowledge of medical terminology and clinical monitoring process Strong ICH-GCPs knowledge Experience with clinical trial information systems Ability to travel up to 60% on average Ability to mentor and train new/junior CRAs on-site in a positive and effective manner What TRIO Can Offer You Competitive salary Paid annual leave Health insurance plan Flexible working hours Luggage allowance Mobile phone allowance Pay Range: 55,000.00 to 65,000.00 Euro - Salary to be influenced (or determined) by the education, experience, location, knowledge, skills, abilities of the applicant, internal equity, and alignment with market data. #
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