Clinical Research Associate-Freelance
Translational Research in Oncology
Summary
TRIO is looking for a Clinical Research Associate (CRA) or Senior Clinical Research Associate (Senior CRA) to join our Monitoring Resources team. This is a remote Independent Contractor opportunity under a one-year contract requiring full-time availability. Applicants must be based in the United States, with preference given to candidates located in the Central or Western regions.
Job description
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
- 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
- Minimum of 1 year monitoring experience on an early phase trial
- Experience monitoring Phase I trials will be valued
- Experience in solid tumor trials, including breast, lung, gastric, ovarian, and/or pancreatic cancer, is preferred
- Fluent in English
- 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 United States
Requirements
- A minimum of 3 years of oncology experience as a CRA, Clinical Research Coordinator, and/or Research Nurse
- Minimum of 1 year monitoring experience on an early phase trial
- Experience monitoring Phase I trials will be valued
- Experience in solid tumor trials, including breast, lung, gastric, ovarian, and/or pancreatic cancer, is preferred
- Fluent in English
- 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 United States
Company overview
Translational Research in Oncology (TRIO) is a unique, full-service oncology clinical research organization (CRO) that specializes exclusively in cancer research. Founded in 1997 and headquartered in Edmonton, Alberta with global hubs in Paris and Montevideo, TRIO operates as a not-for-profit organization focused on accelerating drug development through its translational research model. The company leverages a worldwide network of over 500 highly experienced investigators across more than 20 countries on four continents, supported by academic leaders and patient advocates. TRIO has established a remarkable track record, with 100% of its Phase III trials enrolling on time and four registration trials leading to FDA-approved cancer treatments that have changed clinical practice. The organization's unique structure allows it to focus entirely on patient needs rather than shareholder interests, reinvesting profits to further develop competencies and improve efficiencies in oncology drug development. TRIO's expertise spans from First-in-Human studies to registration trials, with particular strengths in breast cancer research and innovative trial design informed by rigorous preclinical evaluation from its academic partners.