Clinical Research Associate - Freelance

TRIO - Translational Research in Oncology; Edmonton; Remote; CAD 70,000 - 110,000; Full time

Benefits offered by this job

Remote work

Job summary

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.

Responsibilities include data verification, site visits, and ensuring compliance with FDA and ICH-GCP guidelines. The role requires oncology experience, strong regulatory knowledge, and up to 60% travel. French is a plus.

Qualifications

• Minimum 3 years of oncology experience as CRA/CRC/RN.
• Minimum 1 year monitoring experience in early-phase trials.
• Solid tumor trials (breast, lung, gastric, ovarian, pancreatic) preferred.
• Fluent English; French desirable.
• Science-related Bachelor's degree.
• Strong knowledge of ICH-GCP and medical terminology.
• Willingness to travel up to 60%.
• Authorized to work in the country.

Responsibilities

• Data verification of source documents.
• Site visits: pre-study, initiation, monitoring, termination.
• Ensure compliance with FDA, ICH-GCP and local regulations.
• Implement FDA and ICH-GCP guidelines.
• Participate in budget negotiations and follow-up.
• Data validation and query resolution.
• Mentor junior team members.
• Complete and collect regulatory documents.

Skills

oncology experience

English fluent

travel readiness

regulatory knowledge

clinical monitoring

team mentoring

work authorization

Education

Science-related Bachelor's degree

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

Salary to be influenced (or determined) by the education, experience, location, knowledge, skills, abilities of the applicant, internal equity, and alignment with market data.