Clinical Research Associate

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 organizationdedicated to advancing translational cancer research in the clinical trial setting. Our passionate team is committed to providing cancer treatments of the future to the world of today.TRIO is looking for a Clinical Research Associateto join our Monitoring Resources team. Reporting to a CRA Line Manager, this position will be home-based in France.Responsibilities:Conducting site visits, including pre-study, initiation, monitoring and termination;Confirmingadherence 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;Mentoring junior team members as required.Qualifications:A minimum of 2 years of monitoring experience in oncology trialsFluent in French and EnglishCompletion of a science-related Bachelor’s degree Excellent knowledge of medical terminology and clinical monitoring processStrong ICH-GCPs knowledge Experience with clinical trial information systems Ability to travel up to 60% on averageWhat TRIO Can Offer You:Competitive salary5 weeks of vacation plus paid Christmas ClosureHealth& Life Insurance premiums respectively paid 50% & 100% by TRIOFlexible working hoursHome office allowanceAll interviews are currently being conducted virtually - via phone or video. We thank all candidates for their interest; only those selected for an interview will be contacted.Innovation • Teamwork • Passion •Integrity #J-18808-Ljbffr