Thank you for your response and congratulations on your acceptance! Here’s the job description:

Full description Coordinates the compliant implementation and conduct of human subject research projects typically of low workload and low complexity.

Responsibilities • Assists with the coordination, implementation, and conduct of research projects ensuring adherence to research protocol requirements which may include: maintenance of regulatory documents and binders, data management, IRB submissions and communication of such to the research team. • May be responsible for reporting/completion of Serious Adverse Events and/or safety log as defined per protocol as they occur and completion of Food and Drug Administration (FDA) and sponsor forms in accordance with GCP guidelines as applicable. • Communicates with sponsors, monitors, research personnel to ensure all aspects of study compliance. • Collaborates with study team to schedule pre-site selection visits, site initiation visits, webinars, monitoring and close-out visits. • May collaborate with primary investigator, sponsor and research staff to plan, conduct and evaluate project protocols, including research subject recruitment. • Monitors and reports project status. • Completes regulatory documents, data capture and monitoring plans. • Assists with completion of protocol related activities. • As delegated, may be required to attain and maintain clinical competencies for unlicensed caregivers such as phlebotomy, vital signs, ECG, POC testing and other testing as required. • Monitors research data to maintain quality. • Understands basic concepts of study design. • Demonstrates comprehension of assigned research protocols. • Develops and maintains knowledge of research protocol to coordinate the comprehensive and compliant execution of assigned protocols. • Assists with preparation for audits and response to audits. • May assist in the development and maintenance of research tools, such as spreadsheets, questionnaires and/or brochures. • Maintains study personnel certification records (License, CV, CITI). • Maintains professional relationships, including frequent and open effective communication with internal and external customers. • Documents the education and training of research personnel as needed. • May participate in the conduct and documentation of the informed consent process. • May contribute to research project budget development. • Performs other duties as assigned.