Study Coordinator

POSITION RESPONSIBILITIES

• The Study Coordinator assists the Principal Investigator with the management of the recruitment of study participants and collection of data.
• Work with Principal Investigator to refine and finalize research protocols, draft study questionnaires and data collection tools;
• Assist throughout IRB approval process;
• Implement study protocols;
• Perform data collection and quality control of study data;
• Oversee the process by which participants are recruited into the study, adherence to research protocols in obtaining informed consent,blood drawing and testing, data collection and management and participant confidentiality;
• Develop and implement methods to track and follow-up with study participants;
• Coordinate data safety monitoring and produce quarterly reports;
• Oversee questionnaires for completeness and accuracy;
• Arrange meetings of study partners, develop meeting agendas,and facilitate meeting;
• Implement quality control procedures;
• Assist in the preparation of grants for future studies;
• Develop and manage REDCap database.

QUALIFICATIONS

Maximum Salary Range

USD $58,500.00 / Yr.

ABOUT US

This position is in the Division of Nephrology, with a primary assignment to the clinical studies in chronic kidney disease working with the principal investigator. Current kidney studies include studies of complications of kidney disease and improving kidney health. The Study Coordinator assists the Principal Investigator with managing the recruitment of study participants and collection of data.