Senior Oncology Clinical Research Coordinator
University of Oklahoma • Oklahoma City, OK4d • $46,500 - $60,500
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Sr. Oncology Clinical Research Coordinator - CTO
University of Oklahoma•Oklahoma City, OK
•$46,500 - $60,500
About The Position
The Clinical Trials Office at OU Health Stephenson Cancer Center is seeking a highly skilled Senior Oncology Clinical Research Coordinator to support advanced clinical oncology research initiatives. The role helps ensure the accuracy, integrity, and regulatory compliance of clinical trials that contribute to cancer treatment and patient care. The coordinator plans, coordinates, and oversees oncology clinical research activities, ensuring adherence to study protocols, institutional guidelines, and federal regulations. The role includes collecting, evaluating, and analyzing clinical data and preparing documentation required for study conduct and reporting. It requires strong organizational skills, meticulous attention to detail, and effective collaboration with investigators, clinical staff, and research partners. The position contributes to nationally recognized oncology research efforts and 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 substitute for the degree, using a one-to-one ratio to determine years of experience 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 research activities adhere 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.
- Support the accuracy, integrity, and regulatory compliance of clinical trials.
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What This Job Offers
Job Type
Full-time
Career Level
Senior
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