Research Program Coordinator
About The Position
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.
Requirements
- Bachelor's degree in Nursing or Health Professions field, AND:
- 24 months experience in nursing, healthcare, or clinical trials management.
- Equivalent/Substitution: Will accept 48 months equivalent experience in lieu of a Bachelor's Degree.
- Knowledge of project management.
- If the department requires an RN or Physician Assistant, the applicant must have current State licensure.
Responsibilities
- 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.
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What This Job Offers
Job Type
Full-time
Number of Employees
5,001-10,000 employees
