At a Glance
- Tasks: Verify data, conduct site visits, and ensure compliance with regulations in oncology trials.
- Company: Join TRIO, a global leader in advancing cancer research through innovative clinical trials.
- Benefits: Remote work, competitive salary, and the chance to make a real difference in cancer treatment.
- Other info: Flexible freelance role with opportunities for mentorship and professional growth.
- Why this job: Be part of a passionate team dedicated to transforming cancer care for patients worldwide.
- Qualifications: 3+ years in oncology research and strong knowledge of clinical monitoring processes required.
The predicted salary is between 72000 - 88000 $ per year.
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.
Salary to be influenced (or determined) by the education, experience, location, knowledge, skills, abilities of the applicant, internal equity, and alignment with market data.
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.
Clinical Research Associate in Edmonton 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
