Clinical Research Coordinator - ONC Radiation Oncology
Clinical Research Coordinator - ONC Radiation Oncology
Employer Active
Job Alert
You will be updated with latest job alerts via email
Share
Job Alert
You will be updated with latest job alerts via email
$ 58656 - 86000
1 Vacancy
Job Description
Department:
SOM KC Radiation Oncology-----
Radiation OncologyPosition Title:
Clinical Research Coordinator - ONC Radiation OncologyJob Family Group:
Professional StaffJob Description Summary:
This position is responsible for working collaboratively with multidisciplinary teams research and hospital staff to recruit screen educate and assist in the overall clinical study coordination of clinical research. The Clinical Research Coordinator will manage clinical research studies by coordinating and participating in a variety of complex activities involved in the collection compilation documentation and analysis of clinical research data. Monitor participants progress including documenting and reporting adverse events. Participate in periodic quality assurance audits of protocols.Job Description:
Key Roles and Responsibilities
Recruit evaluate and educate patients regarding clinical trials related to radiation oncology disease.
Manages all aspects of study visit activities for patients and families including scheduling of procedures and assessments.
Conduct informed consent interview with participants.
Maintain trial regulatory documentation including correspondence with sponsor KUMC local IRB and central IRB in a timely and accurate manner.
Maintain trial regulatory documentation including correspondence with sponsor KUMC local IRB and central IRB in a timely and accurate manner.
Ensure all study data is entered into sponsored-provided and/or internal KU databases per requirements.
Perform subject visit procedures as needed per education and training. Gather accurate medical history concomitant medication information and ensure that medical conditions meet trial specifications.
Obtain complete reports of new symptoms/changes in health conditions and review with clinician/principal investigator.
Maintain source documents and submit case report forms as required for clinical trials.
Assist clinical staff with sample collection process handling and shipping as outlined in the protocol and within institutional/KUMC policy.
Prepare documentation and participate in study monitoring visits reviews and audits. Provide written and verbal reports to PI and project manager.
Participate in quality assurance activities by reviewing clinical data in medical record charts assessing pharmacy compliance with protocol criteria and reviewing study documentation to ensure compliance with GCP guidelines and FDA CFR.
Provide back-up to other CRC in their absence and all other duties assigned by supervisor.
Prepare documentation for clinical trial feasibility and site qualification visits.
Assist with protocol composition and study design for department investigator-initiated trials.
This job description is not designed to cover or contain a comprehensive listing of activities duties or responsibilities that are required of the employee for this job. It is only a summary of the typical functions of the job not an exhaustive list of all possible job responsibilities tasks duties and assignments. Furthermore job duties responsibilities and activities may change at any time with or without notice.
Required Qualifications
Education
BS in basic science or health related field.
Experience may substitute for degree on a year for year basis.
Work Experience
Minimum of one year experience in a clinical research role or two years healthcare experience with patient interaction or related experience.
Preferred Qualifications
Work Experience
Prior health care and/or research experience.
Familiarity with electronic medical records.
Experience in Radiation Oncology.
Skills
Excellent communication writing organizational and presentation skills.
Required Documents
Resume
Cover Letter
Comprehensive Benefits Package:
Coverage begins on day one for health dental and vision insurance and includes health expense accounts with generous employer contributions if the employee participates in a qualifying health plan. Employer-paid life insurance long-term disability insurance and various additional voluntary insurance plans are available. Paid time off including vacation and sick begins accruing upon hire plus ten paid holidays. One paid discretionary day is available after six months of employment and paid time off for bereavement jury duty military service and parental leave is available after 12 months of employment. A retirement program with a generous employer contribution and additional voluntary retirement programs (457 or 403b) are available. Type: Regular Compensation Statement: The pay range listed for this position is determined by our compensation program using market data and salary benchmarking. A combination of factors is considered in making compensation decisions including but not limited to education experience and training qualifications relative to the requirements of the position and funding. At the University of Kansas Medical Center a reasonable estimate for the starting pay range will be the minimum to midpoint of the posted range taking into account the combination of factors listed above. Minimum Midpoint MaximumTime Type:
Full timeRate Type:
SalaryPay Range:
$58656.00 - $86000.00
Required Experience:
IC
Employment Type
Full-Time
Similar Jobs
Dr. Job is an online platform that connects employers with skilled job seekers, facilitating the search for job opportunities and top talent. Established in 2015. Dr. Job Pro has emerged as the world premier job portal, attracting thousands of job seekers every day from all over the world.
Follow Dr.Job
Dr Job FZ LLC. 2025 © All Rights Reserved