Research Program Coordinator

Oklahoma City, OK - USA

Monthly Salary: Not Disclosed

Posted on: 14 days ago

Vacancies: 1 Vacancy

Job Summary

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.

Important: ALL required documents must be attached to your job application or your documents will not be visible to the hiring department!

Required Education: Bachelors 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 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:

Standard Office Environment

Why You Belong at the University of Oklahoma:The University of Oklahoma values our communitys unique talents perspectives and experiences. At OU we aspire to harness our innovation creativity and collaboration for the advancement of people everywhere. You Belong Here!

Equal Employment Opportunity Statement:The University in compliance with all applicable federal and state laws and regulations does not discriminate on the basis of race color national origin sex sexual orientation marital status genetic information gender identity/expression (consistent with applicable law) age (40 or older) religion disability political beliefs or status as a veteran in any of its policies practices or procedures. This includes but is not limited to admissions employment housing financial aid and educational services.

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.

Required Experience:

Required AttachmentsDocuments 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.Important: ALL required documents must be attached to your job application or your docu...