Sr. Oncology Clinical Research Coordinator - CTO

University of Oklahoma•Oklahoma City, OK

About The Position

The Clinical Trials Office at the Stephenson Cancer Center is seeking a highly skilled Senior Oncology Clinical Research Coordinator to support advanced clinical oncology research initiatives. The position plays a critical role in ensuring the accuracy, integrity, and regulatory compliance of clinical trials that contribute to the advancement of cancer treatment and patient care. The coordinator plans, coordinates, and oversees oncology clinical research activities, including adherence to study protocols, institutional guidelines, and federal regulations. The role also involves collecting, evaluating, and analyzing clinical data, and preparing documentation required for study conduct and reporting. The position requires strong organizational skills, meticulous attention to detail, and effective collaboration with investigators, clinical staff, and research partners. This role offers the opportunity to contribute to nationally recognized oncology research and support the development of innovative therapies intended to improve patient outcomes.

Requirements

  • Bachelor's degree in a health profession, physical science, or biological science, or qualification as a registered nurse or physician assistant.
  • 48 months of clinical practice, nursing, or research program coordination experience.
  • Experience or a combination of education and related experience may be considered in lieu of a degree, using a one-to-one ratio to determine the years of experience required in place of a degree.
  • Strong organizational skills.
  • Meticulous attention to detail.
  • Ability to collaborate effectively with investigators, clinical staff, and research partners.

Responsibilities

  • Plan, coordinate, and oversee oncology clinical research activities.
  • Ensure adherence to study protocols, institutional guidelines, and federal regulations.
  • Collect, evaluate, and analyze clinical data.
  • Prepare documentation required for study conduct and reporting.
  • Collaborate with investigators, clinical staff, and research partners.

Benefits

  • Benefits eligible; specific benefits are not listed.
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