The Stephenson Cancer Center at the University of Oklahoma is the Oklahoma's only National Cancer Institute-Designated Cancer Center, the highest national accreditation for outstanding patient care and research. The Stephenson Cancer Center is the largest oncology practice in the state, with more than 70 board-certified oncology physicians and a large team of advanced providers and supportive care specialists delivering the highest standard of patient-centered, multidisciplinary care for every type of cancer. The Stephenson Cancer Center currently ranks number one among all cancer centers in the nation for the number of patients participating in NCI-sponsored treatment trials, and it is one of only 30 lead centers in the NCI’s National Clinical Trials Network.

The Stephenson Cancer Center is Oklahoma’s leading cancer research organization, with 120 research scientists working to eliminate cancer through conducting innovative basic, clinical and population-based research. These researchers are supported by more than $60 million in annual grant funding from the National Institutes of Health and other sponsors. With a legislatively mandated mission to provide statewide leadership in addressing Oklahoma’s cancer burden, the Stephenson Cancer Center supports numerous outreach, education and screening programs in partnership with the Oklahoma Tobacco Settlement Endowment Trust, the American Cancer Society, the Susan G. Komen Foundation and Oklahoma’s Tribal Nations among many other aligned organizations.

At the Stephenson Cancer Center, we have an exciting new job opportunity that could be right for you! The 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.

Responsibilities:

• Patient Recruitment and Scheduling. Identifies, recruits, and schedules patients who may be eligible to participate in the oncology clinical research program.
• Assessment. 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.
• Testing and Training. Conducts research tests and supervises exercise training sessions.
• Information Distribution. Provides potential patient participants with study information. Obtains informed consent forms.
• Clinical Resource. Acts as the initial clinical resource and liaison between physicians, nurses, and laboratory personnel.
• Data Management. Responsible for data management and data analysis. Ensures data entry is accurate and completed in a timely manner.
• Follow‐Up. 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.
• Meeting Attendance. May attend various meetings pertaining to the oncology clinical research program. May present information at the meeting.
• Personnel Supervision. Assumes lead role to ensure adherence to protocol. Directs and evaluates the work of research personnel. Trains and schedules workloads of employees.
• As Needed. Performs various duties as needed to successfully fulfill the function of the position.

Required Education: Bachelor’s Degree in a health profession or related field

Required Experience: 24 months of clinical practice, nursing, or research program coordination experience.

Equivalent/Substitution: Will accept 48 months of equivalent experience in lieu of a Bachelor’s Degree for a total of 72 months related experience.

Certifications/Licenses: Oklahoma State licensure is required for Nurses and Physician Assistants

Skills:

• 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 acon while following established standards.
• Ability to learn and function under different situations/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

Working Conditions:

Physical: Sitting for prolonged periods. Manual dexterity. Use of a computer and answer telephones.

Environmental: Standard Office Environment.

For more information, visit our website at www.jobs.ou.edu. If you would like to apply, the application must be completed on OUHSC’s job site. The listing for this position is job number 223189 – Oncology Clinical Research Coordinator.

The University if an equal opportunity institution. www.ou.edu/eoo

Job Type: Full-time

Pay: $39,500.00 - $50,400.00 per year

Benefits:

• Dental insurance
• Employee assistance program
• Employee discount
• Flexible spending account
• Health insurance
• Health savings account
• Life insurance
• Paid time off
• Vision insurance

Schedule:

• 8 hour shift
• Day shift

Ability to commute/relocate:

• Oklahoma City, OK 73104: Reliably commute or planning to relocate before starting work (Required)

Education:

• Bachelor's (Preferred)

Experience:

• research program coordination, or clinical: 2 years (Required)

License/Certification:

• Oklahoma State licensure (Required)

Work Location: One location

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