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Oncology Research Coordinator CTO (Tulsa)
Oncology Research Coordinator CTO (Tulsa)The University of Oklahoma • Tulsa, Oklahoma, USA
Oncology Research Coordinator CTO (Tulsa)

Oncology Research Coordinator CTO (Tulsa)

The University of Oklahoma • Tulsa, Oklahoma, USA
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OU Health Stephenson Cancer Center is Oklahomas 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 Stephenson Cancer Center at Hilcrest Utica Park Clinic we have an exciting new job opportunity that could be right for you! 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 evaluates and analyzes clinical data.

To learn more about SCCs Clinical Trials Office (CTO) click here.

Duties :

  • 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.
  • FollowUp. Responsible for the initiation organization and handling of patient followup. Assesses and analyzes patient monitor data at all followup visits. May oversee the conduct of homebased 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 Attachments

Documents required for this position are listed under the Required Attachments section of this job listing. You will be required to upload and attach these documents in the application process.

Important : ALL required documents must be attached to your job application or your documents will not be visible to the hiring department!

Required Education : Bachelors 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 os used to determine the number of years of experience required in place of a degree.

    Certifications / Licenses : None

    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.

    Department Preferences : Phlebotomy experience.

    Why You Belong at the University of Oklahoma : The University of Oklahoma values our communitys unique talents perspectives and experiences. At OU we aspire to harness our innovation creativity and collaboration for the advancement of people everywhere. You Belong Here!

    Equal Employment Opportunity Statement : The University in compliance with all applicable federal and state laws and regulations does not discriminate on the basis of race color national origin sex sexual orientation marital status genetic information gender identity / expression (consistent with applicable law) age (40 or older) religion disability political beliefs or status as a veteran in any of its policies practices or procedures. This includes but is not limited to admissions employment housing financial aid and educational services.

    Required Experience :

    Chief

    Key Skills

    Hospital Experience,Acute Care,Basic Life Support,ICU Experience,Infusion Experience,Triage,TFS,Conflict Management,Nursing,Critical Care Experience,Epic,Medication Administration

    Employment Type : Full-Time

    Experience : years

    Vacancy : 1

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