Clinical Data 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 academic clinical research organization dedicated to advancing translational cancer research in the clinical trial setting. TRIO is looking for a Clinical Research Associate to join our Monitoring Resources team. Reporting to a CRA Line Manager, this position will be home-based in Eastern Canada. 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; Assisting with data validation and query resolution; A minimum of 2 years of monitoring experience in oncology trials Fluent in English and French Experience monitoring phase 1 trials An advanced level of oncology knowledge Completion of a science-related Bachelor’s degree Excellent knowledge of medical terminology and clinical monitoring process Experience with clinical trial information systems Ability to travel up to 60% on average Fluent in both English and French Competitive salary ~3 weeks of vacation plus paid Christmas Closure ~2 weeks paid personal/sick time ~ Health, Dental, Vision & Life Insurance premiums paid by TRIO ~ Flexible

working hours
~ Pay Range $105,000.00 to $140,000.00 annually
- Salary to be influenced (or determined) by the education, experience, location, knowledge, skills, abilities of the applicant, internal equity, and alignment with market data.