Sr Clinical Research Coordinator
Job Description
Come join the staff at OU HSC and become a part of Oklahoma's premier research university which leads the state in education and career opportunities. OU HSC is one of only four comprehensive academic health centers in the nation with seven professional colleges.
This position coordinates a clinical research program by identifying and assessing patients, distributing information, acting as a clinical resource, managing data, conducting follow-up care for patients, attending meetings pertaining to the program, and supervising program personnel.
Duties:
- Identifies patients who may be eligible to participate in the research program
- Performs the initial assessment of potential patients
- Obtains clinical history and completes patient data forms
- Provides potential patients with study information
- Obtains informed consent forms
- Acts as the immediate clinical resource and the liaison between physicians, nurses, laboratory personnel, etc.
- Performs data management and data analysis
- Responsible for the initiation, organization, and carrying out of patient follow-up
- Assesses patients at all follow-up visits.
- Attends various meetings pertaining to the research program
- May present information
- May assume the lead role when the supervisor is not available to ensure adherence to protocol
- May lead and train research personnel
- Performs various duties as needed to successfully fulfill the function of the position
Job Requirements
Required Education: Bachelor's Degree in a Health Profession, Physical Science, Biological Science, or Registered Nurse OR Master's Degree in Physician Assistant AND:
- 48 months of clinical practice, nursing, or research program coordination experience.
Equivalent/Substitution: Will accept 48 months clinical practice or research program coordinator experience in lieu of the Bachelor's Degree for a total of 96 months experience.
Certifications / Licenses:
- Registered Nurse Licensure through the Oklahoma Board of Nursing
- Physician Assistant Licensure through the Oklahoma Medical Board
Skills:
- Working knowledge of clinical trials protocols
- Proficient with Microsoft Office to include Outlook, Excel, Outlook, or PowerPoint
- Ability to communicate verbally or in writing
- Detail oriented
- Ability to lead and train other employees.
Working Conditions:
- Physical: Sitting for prolonged periods. Manual dexterity. Reaching, speaking, and listening.
- Environmental: Standard Office Environment.
Whoops! This job is not yet sponsored…
Or, view more options below
View full job details
See the complete job description, requirements, and application process
Express interest in this position
Let University of Oklahoma know you're interested in Sr Clinical Research Coordinator
Get similar job alerts
Receive notifications when similar positions become available







