Clinical Research Coordinator - Open Rank
About the position Responsibilities • Obtain consent of research participants in accordance with IRB approved protocols and regulations including HIPAA. • Identify, schedule and/or conduct participant study visits, tests, and interviews. • Coordinate participant remuneration/compensation per protocol. • Maintain all regulatory documentation, including IRB and study data. • Identify issues with protocol compliance and keep the PI and manager informed. • Document and collect data and/or samples during participant study visits. • Ensure accurate documentation of study activities by clinicians and/or PI. • Track and maintain study enrollment and completion of milestones. • Assist with financial/operational aspects of grants and contracts. • Monitor inventory of research-related supplies. • Participate in grant preparation, manuscript writing, and IRB processes. • Provide written summaries from literature searches for the study team. • Present study status reports related to assigned research projects. • Participate in the design and documentation of study-related data collection tools. • Maintain strict adherence to study protocols and regulatory requirements. Requirements • Bachelor's degree in a scientific or health-related field, or equivalent experience. • 0-1 year of related experience for Clinical Research Coord I. • 1-3 years of related experience for Clinical Research Coord II. • 3-5 years of related experience for Clinical Research Coord III. • 5-7 years of related experience for Sr Clinical Research Coord. • Ability to travel to off-site locations. Apply tot his job Apply tot his job