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, part-time freelance opportunityon a6-month contract, open to candidates based in Canada.
Responsibilities
- Performing 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 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 2 years of monitoring experience in oncology trials
- Fluent in French and English
- Experience monitoring in early-phase trialswill be valued.
- 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.