Clinical Research Coord I

Obtain consent of research participants in accordance with IRB approved protocols and all applicable regulations. Identify, schedule, and conduct participant study visits, interviews, and tests while coordinating participant remuneration. Maintain regulatory documentation, including IRB and study data, and provide support to Investigators, sponsors, and external monitors. Document and collect data and samples during study visits, track enrollment and completion milestones, and monitor research supply inventory. Assist with financial and operational aspects of grants and contracts, including billing review. Participate in grant preparation, manuscript writing, and IRB processes, while presenting study status reports and providing literature summaries to the team. Design and document data collection tools, ensure strict adherence to Good Clinical Practice guidelines, and maintain confidentiality.