*Sr. Clinical Research Coordinator

Posted: Friday, 08 August 2025
Valid Thru: Sunday, 07 September 2025
Index Requested on: 08/09/2025 01:53:57
Indexed on: 08/09/2025 01:53:57

Location: Oklahoma City, OK, 73101, US

Industry: Education
Occupational Category: 11-0000.00 - Management
Type of Employment: FULL_TIME

University of Oklahoma is hiring!

Description:

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, and attending meetings pertaining to the program.

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.

Responsibilities:

Please review the job description.

Educational requirements:

  • high school

Desired Skills:

Required Education: Bachelor's Degree in a Health Profession, Physical Science, Biological Science, or Registered Nurse, OR Master's Degree in Physician Assistant

  • 48 months of clinical practice, nursing, or research program coordination experience.

Equivalency Substitution: Will accept 48 months clinical practice or research program coordinator experience in lieu of the Bachelors Degree for a total of 96 months of experience.

Skills:

  • Working knowledge of clinical trials protocols and GCP.
  • Proficient with Microsoft Office to include Outlook, Excel, or PowerPoint.
  • Ability to communicate verbally or in writing.
  • Detail oriented with excellent organizational skills.
  • Ability to lead and train other employees.

Certifications:

  • If applicable, Registered Nurse Licensure through the Oklahoma Board of Nursing

  • Physician Assistant Licensure through the Oklahoma Medical Board.

Working Conditions:

  • Physical:
    • Sitting for prolonged periods.
    • Manual dexterity.
    • Reaching, speaking, and listening.
  • Environmental:
    • Standard Office Environment.

Departmental Preferences:

  • Experience with IRB submissions and studies.
  • CCRP Certification.

Why You Belong at the University of Oklahoma: The University of Oklahoma values our community's 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.


Benefits:

Please see the job description for benefits.

Apply Now