Full-Time

Oncology Research Coordinator

Cto

Posted on 10/31/2025

University of Oklahoma

University of Oklahoma

No salary listed

Oklahoma, USA

In Person

Category
Medical, Clinical & Veterinary (2)
,
Required Skills
Data Analysis
Requirements
  • Bachelor’s Degree in a health profession or related field, AND 24 months of research program coordination, or clinical experience.
  • Equivalent/Substitution: Experience or a combination of education & related 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.
  • Certifications/Licenses: Oklahoma State licensure is required for Nurses and Physician Assistants
  • Skills: Advanced knowledge of protocol guidelines, principles, and practices.
  • Skills: Must have a high level of organizational skills.
  • Skills: Ability to exercise discretion.
  • Skills: Ability to ask the right questions to determine proper course of action while following established standards.
  • Skills: Ability to learn and function under different situations/circumstances.
  • Skills: Must work independently and as a team member.
  • Skills: Ability to handle stressful situations and solve problems.
  • Skills: Ability to finish projects in a timely manner
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.
University of Oklahoma

University of Oklahoma

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