Cancer Outcomes Research Program Coordinator

University of OklahomaOklahoma City, OK
$38,700 - $50,300Onsite

About The Position

OU Health Stephenson Cancer Center is Oklahoma's only National Cancer Institute (NCI)-Designated Cancer Center, and one of only 74 NCI-Designated Cancer Centers in the United States. This highly competitive accreditation ensures that our patients receive the highest standard of care and have access to the most advanced cancer treatment options. Join the Future of Cancer Research at the Stephenson Cancer Center! Are you ready to make a meaningful impact in the lives of patients and families affected by cancer? At the Stephenson Cancer Center, we're thrilled to announce an exciting opportunity to join our team as a Cancer Outcomes Research Program Coordinator, a role designed for someone who's passionate about advancing cancer care through innovative research. As a key member of our Cancer Outcomes Research Program, you'll be at the heart of studies that shape the future of symptom management, supportive care, digital health, and long term cancer outcomes. This is your chance to contribute to groundbreaking work while collaborating with leading clinicians, researchers, and principal investigators.

Requirements

  • Bachelor's degree in Nursing or Health Professions field.
  • 24 months experience in nursing, healthcare, or clinical trials management.
  • Will accept 48 months equivalent experience in lieu of a Bachelor's Degree.
  • If the department requires an RN or Physician Assistant, the applicant must have current State licensure.

Responsibilities

  • Coordinate multiple research protocols and projects that drive real-world impact
  • Engage directly with participants, screening, consenting, enrolling, and supporting them throughout the study
  • Manage essential research data using REDCap and OnCore
  • Partner with the Institutional Review Board on protocol development, submissions, and updates
  • Identify recruitment barriers and help shape strategies to overcome them
  • Assist in developing study materials, maintaining regulatory documentation, and tracking study progress
  • Conduct medical record reviews and contribute to manuscript development
  • Work closely with 2-3 principal investigators and collaborate with a dynamic team of Research Assistants, Project Managers, clinicians, and scientists

Benefits

  • Benefits Eligible: Yes
© 2026 Teal Labs, Inc
Privacy PolicyTerms of Service