Research Program Coordinator

Coordinates and administers multiple clinical research projects by performing clinical research, medical management, subject recruitment, data analysis, IRB Coordination, counseling and education.

Duties :

Coordinates the activities between clinical research projects for a department or college and between those projects and other programs on the national or state level.

• Works with academic and clinical staff to develop clinical research, testing, and training materials.
• Assists clinical investigators in planning, organizing, and delivering medical management of study participants.
• Performs medical record reviews, establishes preliminary diagnosis and orders laboratory and non-invasive x-ray tests.
• Recruits subjects for clinical research projects.
• Reviews medical histories and may examine subjects to determine eligibility.
• Enrolls subjects meeting criteria of the project.
• Organizes and participates in the analysis of collected data.
• May perform data entry, collect, analyze, and clean data.
• Works with the Institutional Review Board to develop protocols and consent forms for research projects including human subjects.
• Ensures projects are in compliance with University regulations.
• Provides counseling and education to the subject and family concerning the research project, and the management orprevention of health disorders.
• Trains support personnel in new techniques, requirements, and procedures necessary for research protocols, protectingsubject safety, and ensuring the integrity of data.
• Performs various duties as needed to successfully fulfill the function of the position.