Clinical Research Associate-Freelance

If you are an experienced CRA who is passionate about oncology research and looking to join a highly skilled and knowledgeable team, TRIO could be the place for you! 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 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 opportunityunder 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. 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 guidelinesAssisting with data validation and query resolutionMentoring junior team members as requiredEnsuring 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 trialExperience monitoring Phase I trialswill be valued.Experience in solid tumor trials, including breast, lung, gastric, ovarian, and/or pancreatic cancer, is preferred;Fluent in EnglishCompletion of a science-related Bachelor’s degreeExcellent knowledge of medical terminology and clinical monitoring processStrong ICH-GCPs knowledgeExperience with clinical trial information systemsAbility to travel up to 60% on averageMust be legally authorized to work in the United States. The contract rate and seniority level will be determined based on the applicant’s education, relevant experience, location, knowledge, skills, and abilities, as well as internal equity and market data. If you are ready to take the next step in your oncology clinical research career and contribute to meaningful cancer research, we would love to hear from you!