"Oncology Clinical Research Coordinator - CTO"

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.

The Oncology Clinical Research Coordinator - CTO plans, directs, or coordinates clinical oncology research projects, directs the activities of workers engaged in clinical oncology research projects to ensure compliance with protocols and overall clinical objectives, and evaluates and analyzes clinical data.

To learn more about SCC's Clinical Trials Office (CTO), click here.

Duties:

• Identifies, recruits, and schedules patients who may be eligible to participate in the oncology clinical research program.
• Performs the initial assessment of potential patient participants, including taking detailed clinical history, performing physical exam, and completing patient data forms.
• Conducts research tests and supervises exercise training sessions.
• Provides potential patient participants with study information and obtains informed consent forms.
• Acts as the initial clinical resource and liaison between physicians, nurses, and laboratory personnel.
• Responsible for data management and data analysis, ensuring data entry is accurate and completed in a timely manner.
• Responsible for the initiation, organization, and handling of patient follow-up, assessing and analyzing patient monitor data at all follow-up visits, and may oversee home-based patient training programs.
• May attend various meetings pertaining to the oncology clinical research program and present information.
• Assumes lead role to ensure adherence to protocol, directs and evaluates the work of research personnel, and trains and schedules workloads of employees.
• Performs various duties as needed to successfully fulfill the function of the position.

Job Requirements: Required Education: Bachelor's Degree in a health profession or related field, and 24 months of research program coordination or clinical experience. Equivalent substitutions may be considered. Certifications/Licenses: None. Skills: Advanced knowledge of protocol guidelines, high organizational skills, ability to exercise discretion, work independently and in teams, handle stressful situations, and finish projects timely. Working Conditions: Physical - Sitting for prolonged periods, manual dexterity, use of computer and answering telephones. Environmental - Standard office environment.

Salary Range: Targeted annual salary from $39,500 to $50,400, based on experience. Benefits Provided: Yes. Required Attachments: Resume. Work Schedule: Monday-Friday 8am-5pm. Work Type: Onsite.