Sr. Oncology Clinical Research Coordinator - CTO

University of Oklahoma • Oklahoma City, OK

11d

About The Position

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 Senior Oncology Clinical Research Coordinator 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, evaluates and analyzes clinical data. Learn more about the Stephenson Cancer Center’s Clinical Trials Office here.

Requirements

• Bachelor’s Degree in Health Profession, Physical Science, Biological Science, Registered Nurse, Physician Assistant, AND:
• 48 months of clinical practice, nursing, or research program coordination experience.
• Equivalency/Substitution: Experience or a combination of education & experience can be considered in lieu of a degree. A one-to-one ratio is used to determine the number of years of experience required in place of a degree.
• Advanced knowledge of protocol guidelines, principles, and practices.
• Must have a high level of organizational skills.
• Ability to exercise discretion.
• Ability to ask the right questions to determine proper course of action while following established standards.
• Ability to learn and function under different situation and circumstances.
• Must work independently and as a team member.
• Ability to handle stressful situations and solve problems.
• Ability to finish projects in a timely manner.

Responsibilities

• 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 but not limited to 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. 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. Ensures data entry is accurate and completed in a timely manner. Responsible for the initiation, organization, and handling of patient follow‐up. Assesses and analyzes patient monitor data at all follow‐up visits. May oversee the conduct of home‐based patient training programs.
• May attend various meetings pertaining to the oncology clinical research program. May present information at the meeting.
• Assumes lead role to ensure adherence to protocol. Directs and evaluates the work of research personnel. Trains and schedules workloads of employees.
• Performs various duties as needed to successfully fulfill the function of the position.

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level
• Number of Employees: 5,001-10,000 employees