OU Health Stephenson Cancer Center is Oklahoma’s only National Cancer Institute (NCI)-Designated Cancer Center, and one of only 73 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.

At the Stephenson Cancer Center, we have an exciting new job opportunity that could be right for you! The Cancer Rehabilitation Research Laboratory (CRRL) Cancer Rehab Research Coordinator assists with research projects, ensures compliance with protocols and overall research objectives, evaluates the integrity of clinical data, and assists with preparing the data for analysis. Uses knowledge of scientific procedures to plan, design, conduct, and analyze experiments. The CRRL Research Coordinator works under the direct oversight of the SCC CRRL Program Director and Study PI, but must make real-time decisions for successful study conduct.

Duties:

• Planning, scheduling, and recruitment of patients who may be eligible to participate in the oncology clinical research program.
• Monitoring human performance assessments and making observations, including but not limited to taking detailed clinical history, performing physical exams, and completing patient data forms.
• Performing routine or standardized research tests and supervising exercise training sessions.
• Responsible for the initiation, organization, and handling of patient follow-up.
• Preparing clinical data for analysis, presentation, or examination. Responsible for data management, including entry and storage in both paper and electronic mediums. Ensuring data are accurate and entry is completed in a timely manner.
• Conducting special research studies.
• Troubleshooting, modifying, and repairing experimental and laboratory products.
• Preparing reports summarizing the results of experiments or the conclusions of research projects.
• Cleaning, maintaining, and preparing supplies and work areas.
• Keeping detailed records of all work-related activities.
• May publish research.
• May requisition or recommend purchase of materials, tools, and equipment.
• May attend various meetings pertaining to the oncology clinical research program. May work to schedule meetings, create agendas, and record meeting notes/minutes for these meetings.
• Conducts research of literature as needed.
• Develops and assists in the generation of patient participant-facing materials. Creates internal resources to bolster team reliability.
• Assumes lead role to ensure adherence to protocols.
• Performs various duties as needed to successfully fulfill the functions of the position.