[Remote] Clinical Research Associate-Freelance

Note: The job is a remote job and is open to candidates in USA. TRIO - Translational Research in Oncology is a global academic clinical research organization focused on advancing cancer research. They are seeking a Clinical Research Associate to join their Monitoring Resource team, responsible for conducting site visits, ensuring compliance with regulations, and mentoring junior team members.ResponsibilitiesPerforming data verification of source documentsConducting site visits, including pre-study, initiation, monitoring, and terminationConfirming adherence to all FDA, ICH-GCP, and local regulationsEnsuring implementation and compliance with FDA, and ICH-GCP guidelinesParticipating in budget negotiation and follow-up where applicableAssisting with data validation and query resolutionMentoring junior team members as requiredEnsuring the completion and collection of regulatory documentsSkillsA minimum of 2 years of monitoring experience in oncology trialsExperience monitoring in early-phase trials will be valuedCompletion 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 countryCompany OverviewTRIO is an academic clinical research organization that is dedicated to advancing translational cancer research. It was founded in 1997, and is headquartered in Edmonton, Alberta, CAN, with a workforce of 201-500 employees. Its website is http://www.trioncology.org.