Clinical Research Associate 254891

We are looking to add a Clinical Research Associate to a growing team to help monitor an Oncology trial. This role will start around 20-25 hours weekly with the potential to increase to full time toward the beginning of 2027. This study will need mostly remote support with some local travel to sites up to 4-6 times a year. 2 years of non co-monitoring experience is required Previous experience monitoring Oncology studies is required There will be no sponsorship provided for this role Candidates must live in California Resposibilites Act as the primary liaison between the company, the Sponsor, and clinical sites. Verify source data (SDV/SDR) by cross-referencing original medical records with case report forms (CRFs) to maintain accuracy. Manage Trial Master File (TMF) maintenance and reconcile with the Investigator Site File (ISF). Handle query resolution, investigate endpoints, and confirm inclusion/exclusion criteria. Maintain audit-ready clinical sites and track site performance, proposing corrective measures when necessary. Qualifications & Requirements 1 to 2 years of independent monitoring experience (co-monitoring only is not sufficient). Oncology experience is highly preferred. Experience in multicenter Phase III-IV clinical trials is also preferred. Bachelor's degree in Life Sciences, Nursing, Chemistry, Biology, Pharmacy, or a related field. #J-18808-Ljbffr Medix™