Clinical Research Associate - Freelance

Translational Research in Oncology (TRIO)is a global academic 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 seeking a Clinical Research Associate (CRA) to join our Monitoring Resource team. This is a remote, full-time freelance opportunity on a 1-year contract, open to candidates based in Western Canada (British Columbia, Alberta, Saskatchewan, or Manitoba).ResponsibilitiesPerforming data verification of source documents;Conducting site visits, including pre-study, initiation, monitoring, and termination;Confirmingadherence to all FDA, ICH-GCP, and local regulations;Ensuring implementation and compliance with FDA, and ICH-GCP guidelinesParticipating in budget negotiation and follow-up where applicableAssisting with data validation and query resolutionMentoring junior team members as requiredEnsuring the completion and collection of regulatory documents

Qualifications

A minimum of 3 years of oncology experience as a CRA, Clinical Research Coordinator, and/or Research Nurse;A minimum of 1 year of monitoring experience in an early-phase clinical trial;Experience in solid tumor trials, including breast, lung, gastric, ovarian, and/or pancreatic cancer, is preferred;Fluent English required; French is desirableExperience monitoring in phase I trialswill be valueCompletion of a science-related Bachelor’s degreeExcellent knowledge of medical terminology and clinical monitoring processStrong ICH-GCPs knowledgeExperience with clinical trial information systemsAbility to travel up to 60% on averageMust be legally authorized to work in the countryPay Range:$80.00 to $100.00 HourlyHourly Rate to be influenced (or determined) by the education, experience, location, knowledge, skills, abilities of the applicant, internal equity, and alignment with market data.Teamwork Passion Integrity Innovation