*Research Program Coordinator - Job Number: 250479
Job Description
Job Description
---Coordinates and administers multiple clinical research projects by performing clinical research, medical management, subject recruitment, budget preparation, data analysis, IRB Coordination, counseling and education, and personnel supervision.
Duties:
- Project Coordination. 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.
- Clinical Research. Works with academic and clinical staff to develop clinical research, testing, and training materials.
- Medical Management. 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.
- Subject Recruitment. Recruits subjects for clinical research projects. Reviews medical histories and may examine subjects to determine eligibility. Enrolls subjects meeting criteria of the project.
- Budget Preparation. Prepares and manages the budget for clinical research projects sponsored by outside funding sources.
- Data Analysis. Organizes and participates in the analysis of collected data. May perform data entry, collect, analyze, and clean data.
- IRB Coordination. 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.
- Counseling and Education. Provides counseling and education to the subject and family concerning the research project, and the management or prevention of health disorders.
- Personnel Supervision. Supervises support personnel that may include nurses, physician assistants, researchers, technical positions, etc. Delegates tasks, and conducts performance appraisals. Assists Principal Investigator in the selection, and training of new employees. Trains support personnel in new techniques, requirements, and procedures necessary for research protocols, protecting subject safety, and ensuring the integrity of data.
- As Needed. Performs various duties as needed to successfully fulfill the function of the position.
Job Requirements
---Required education: Bachelor’s Degree in Nursing or Health Professions field,AND:
- 24 months experience in nursing, healthcare, or clinical trials management
Equivalency/Substitution: Will accept 48 months of equivalent experience in lieu of a Bachelor's Degree.
Skills:
- Knowledge of project management.
Certifications: If the department requires an RN or Physician Assistant, the applicant must have current State licensure.
Working Conditions:
- Environmental: Standard Office Environment
Why You Belong at the University of Oklahoma:The University of Oklahoma fosters an inclusive culture of respect and civility, belonging, and access, which are essential to our collective pursuit of excellence and our determination to change lives. The unique talents, perspectives, and experiences of our community enrich the learning, and working environment at OU, inspiring us to harness our innovation, creativity, and collaboration for the advancement of people everywhere.
Equal Employment Opportunity Statement:The University of Oklahoma, in compliance with all applicable federal and state laws and regulations, does not discriminate based on race, color, national origin,sex, sexual orientation, genetic information, gender identity, gender expression, age, religion, disability, political beliefs, or status as a veteran in any of itspolicies, practices, or procedures. This includes, but is not limited to, admissions, employment, financial aid, housing, services in educational programs or activities,and health care services that the University operates or provides.
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