*Cancer Rehab Research Coordinator
*Cancer Rehab Research Coordinator
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1 Vacancy
Job Description
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.
Required Education: Bachelors degree. AND:
- 24 months research or laboratory experience.
Equivalency/Substitution: Will accept 48 months of related experience in lieu of the Bachelors degree for a total of 72 months of related experience.
Certifications or Licenses: none.
Skills:
Proficient navigating and maintaining database - Ability to speak read and write clear concise English
- Strong professional oral and written communication skills
- Proficient in Microsoft Office
- Highly organized and able to handle multiple projects and deadlines
- Able to produce reports and complete work within deadlines
- Must be able to read and interpret policy as well as State and Federal regulations
Working Conditions:
- Physical:
- Ability to engage in repetitive motions.
- Must be able to crouch crawl and reach.
- Sitting for prolonged periods.
- Manual dexterity.
- Lift and carry up to 50 lbs.
- Ability to walk for short or extended periods of time.
- Ability to safely guard patient participants to ensure their safety.
- Environmental:
- Research or laboratory environment or in the field & Standard Office Environment.
- Research or laboratory environment or in the field & Standard Office Environment.
Department Preferences: Education in Exercise Science or Human Performance related field is preferred but not required.
Why You Belong at the University of Oklahoma:The University of Oklahoma fosters an inclusive culture of respect and civility belonging and access which are essential to our collective pursuit of excellence and our determination to change lives. The unique talents perspectives and experiences of our community enrich the learning and working environment at OU inspiring us to harness our innovation creativity and collaboration for the advancement of people everywhere.
Equal Employment Opportunity Statement:The University of Oklahoma in compliance with all applicable federal and state laws and regulations does not discriminate based on race color national origin sex sexual orientation genetic information gender identity gender expression age religion disability political beliefs or status as a veteran in any of its policies practices or procedures. This includes but is not limited toadmissions employment financial aid housing services in educational programs or activities and health care services that the University operates or provides.
OU Health Stephenson Cancer Center is Oklahomas only National Cancer Institute (NCI)Designated Cancer Center and one of only 73 NCIDesignated 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 Cancer Rehabilitation Research Laboratory (CRRL) Cancer Rehab Research Coordinator assists with research projects ensures compliance with protocols and overall research objectives evaluates the integrity of clinical data and assists with preparing the data for analysis. Uses knowledge of scientific procedures to plan design conduct and analyze experiments. The CRRL Research Coordinator works under the direct oversight of the SCC CRRL Program Director and Study PI but must make realtime decisions for successful study conduct.
Duties:
Planning scheduling and recruitment of patients who may be eligible to participate in the oncology clinical research program. - Monitoring human performance assessments and making observations including but not limited to taking detailed clinical history performing physical exams and completing patient data forms.
- Performing routine or standardized research tests and supervising exercise training sessions.
- Responsible for the initiation organization and handling of patient followup.
- Preparing clinical data for analysis presentation or examination. Responsible for data management including entry and storage in both paper and electronic mediums. Ensuring data are accurate and entry is completed in a timely manner.
- Conducting special research studies.
- Troubleshooting modifying and repairing experimental and laboratory products.
- Preparing reports summarizing the results of experiments or the conclusions of research projects.
- Cleaning maintaining and preparing supplies and work areas.
- Keeping detailed records of all workrelated activities.
- May publish research.
- May requisition or recommend purchase of materials tools and equipment.
- May attend various meetings pertaining to the oncology clinical research program. May work to schedule meetings create agendas and record meeting notes/minutes for these meetings.
- Conducts research of literature as needed.
- Develops and assists in the generation of patient participantfacing materials. Creates internal resources to bolster team reliability.
- Assumes lead role to ensure adherence to protocols.
- Performs various duties as needed to successfully fulfill the functions of the position.
Required Experience:
IC
Employment Type
Full-Time
