At a Glance
- Tasks: Conduct site visits and ensure compliance with clinical trial regulations.
- Company: Join TRIO, a global leader in cancer research dedicated to innovative treatments.
- Benefits: Competitive hourly pay, remote work flexibility, and opportunities for mentorship.
- Other info: Remote freelance role with potential for career growth in a dynamic environment.
- Why this job: Make a real difference in cancer research while working with a passionate team.
- Qualifications: 3+ years in oncology and monitoring experience in early-phase clinical trials required.
The predicted salary is between 80 - 100 $ per hour.
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 trials will 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.
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
Clinical Research Associate in Vancouver employer: Translational Research in Oncology
At Translational Research in Oncology (TRIO), we pride ourselves on being an exceptional employer that fosters a collaborative and innovative work culture. Our remote, freelance Clinical Research Associate position offers the flexibility to work from anywhere in Western Canada while contributing to groundbreaking cancer research. With a strong commitment to employee growth, we provide opportunities for mentorship and professional development, ensuring that our team members are equipped to make a meaningful impact in the fight against cancer.
Contact Details:
Translational Research in Oncology Recruitment Team
