The CRA will perform data verification, conduct site visits, and ensure compliance with FDA and ICH-GCP guidelines. Responsibilities also include assisting with data validation, query resolution, and collecting regulatory documents.
Translational Research in Oncology (TRIO) is a global academic clinical research organization dedicated 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 seeking a Clinical Research Associate (CRA) to join our Monitoring Resource team. This is a remote, part-time freelance opportunity on a 6-month contract, open to candidates based in Canada.
Salary to be influenced (or determined) by the education, experience, location, knowledge, skills, abilities of the applicant, internal equity, and alignment with market data.
Prior to applying please review TRIO's Applicant Information Notice [https://drive.google.com/file/d/1OmkMw3kKL1z_Hic3hUqE_P34jSxWdEhT/view?usp=sharing]
To support efficiency, TRIO may use limited AI tools during the candidate review process. All hiring decisions are made by people, not AI.
To ensure fairness and an accurate understanding of your skills, we ask that candidates refrain from using AI tools or AI‑generated responses during interviews or assessments. We want the opportunity to get to know you and your experience.
Teamwork · Passion · Integrity · Innovation
Candidates must have a science-related Bachelor's degree and at least 2 years of monitoring experience in oncology trials. Fluency in both French and English and the ability to travel up to 60% are required.
