Clinical Research Associate - Freelance

Freelance; Vancouver; Remote; CAD 110,000 - 138,000; Full time

Job summary

Translational Research in Oncology (TRIO) is seeking a Clinical Research Associate to join the 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 include data verification, site visits (pre-study to termination), regulatory compliance, budget assistance, data validation, mentoring, and ensuring regulatory documents are completed.

Qualifications

• Minimum 3 years oncology experience as CRA/CRC/RN.
• At least 1 year monitoring in early-phase trials.
• Experience in solid tumor trials (breast, lung, gastric, ovarian, pancreatic) preferred.
• Fluent English; French desirable.
• Bachelor’s degree in a science-related field.
• Strong ICH-GCP knowledge and ability to travel up to 60%.

Responsibilities

• Perform data verification of source documents.
• Conduct site visits: pre-study, initiation, monitoring, termination.
• Ensure adherence to FDA, ICH-GCP and local regulations.
• Ensure implementation of FDA and ICH-GCP guidelines.
• Participate in budget negotiation and follow-up.
• Assist with data validation and query resolution.
• Mentor junior team members and collect regulatory documents.

Skills

Oncology CRA experience

Early-phase monitoring

Solid tumor trials

Fluent English

French desirable

Travel up to 60%

Legal work authorization

Medical terminology

ICH-GCP knowledge

Clinical trial systems

Education

Science-related Bachelor’s degree

Tools

Clinical trial information systems

Job description

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).

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 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 trialswill 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

Pay Range:$80.00 to $100.00 Hourly Hourly 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

Prior to applying please review TRIO's Applicant Information Notice

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