Clinical Research Coordinator

Study Coordinator / Clinical Research Specialist Duration: 6 Months Pay Rate: $32.50/hour Schedule: Full-Time (Occasional evenings, weekends, and holidays as needed) Position Summary Seeking an experienced Study Coordinator/Clinical Research Specialist to independently manage multiple oncology clinical trials from startup through closeout. The role involves coordinating study activities, enrolling participants, maintaining regulatory compliance, managing study data, and collaborating with investigators, sponsors, and clinical teams while ensuring adherence to ICH-GCP, FDA, IRB, and institutional guidelines. Key Responsibilities Coordinate Phase I–III oncology clinical trials from activation to closeout. Recruit, consent, enroll, and manage study participants. Maintain regulatory documents, source documentation, and study records. Enter and manage clinical data, resolve queries, and support monitoring visits. Coordinate biospecimen collection, processing, storage, and shipment. Ensure compliance with GCP, FDA, IRB, sponsor, and institutional requirements. Report adverse events, protocol deviations, and support audits. Collaborate with investigators, sponsors, research staff, and clinical teams. Minimum Qualifications Bachelor's degree in a scientific, healthcare, or related field with 1+ year of clinical research experience, or equivalent combination of education and experience. #J-18808-Ljbffr Integrated Resources, Inc ( IRI )