Clinical Research Associate - Freelance

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, full-time freelance opportunity  on a  1-year contract , open to candidates based in  Western Canada  (British Columbia, Alberta, Saskatchewan, or Manitoba).
Responsibilities   Performing data verification of source documents;
Conducting site visits, including pre-study, initiation, monitoring, and termination;
Confirming adherence to all FDA, ICH-GCP, and local regulations;
Ensuring implementation and compliance with FDA, and 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
Ensuring 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 desirable
Experience monitoring in phase I trial swill be value
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
Must be legally authorized to work in the country
Salary to be influenced (or determined) by the education, experience, location, knowledge, skills, abilities of the applicant, internal equity, and alignment with market data.