Research Program Coordinator
Research Program Coordinator
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Salary Not Disclosed
1 Vacancy
Job Description
Required education: Bachelors Degree in Nursing or Health Professions fieldAND:
- 24 months experience in nursing healthcare or clinical trials management
Equivalency/Substitution: Will accept 48 months of equivalent experience in lieu of a Bachelors 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 originsex 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 activitiesand health care services that the University operates or provides.
Required Attachments
Documents required for this position are listed under the Required Attachments section of this job listing. You will be required to upload and attach these documents in the application process.
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 noninvasive xray 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.
Required Experience:
IC
Employment Type
Full-Time
