Clinical Research Coordinator -Cancer Center (Lee's Summit)
Clinical Research Coordinator -Cancer Center (Lee's Summit)
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$ 58656 - 86000
1 Vacancy
Job Description
Department:
SOM KC Cancer Center Clinical TrialsClinical Trials Clinical OperationsPosition Title:
Clinical Research Coordinator Cancer Center (Lees Summit)Job Family Group:
Professional StaffJob Description Summary:
The Clinical Research Coordinator works collaboratively with multidisciplinary teams research and hospital staff to recruit screen educate and assist in the overall clinical study coordination of complex clinical research. This position manages assigned clinical research studies by supervising a variety of complex activities involved in the collection compilation documentation and analysis of clinical research data. This Clinical Research Coordinator monitors participants progress including documenting and reporting adverse events. This role participates in periodic quality assurance audits of protocols.This position will be 100% onsite due to the fact this is a patient facing role. The Lees Summit site is located at: 4881 NE Goodview Cir Lees Summit MO 64064.
The University of Kansas Cancer Center is the only National Cancer Institute designated Comprehensive Cancer Center in the region 1 of only 57 in the nation to receive this distinction. Patients gain access to the most promising therapies cuttingedge clinical trials and world class research.
Job Description:
Job Duties:
Recruit and educate potential patients for and evaluate potential patient eligibility for clinical trials.
Maintain source documents and submit case report forms (CRFs) as required for clinical trials.
Recognize and report adverse events/serious adverse events to the Principal Investigator FDA and sponsors.
Perform study procedures as outlined in the protocol and within state and institutional scope of practice.
Assist clinical staff with phlebotomy and sample collection processing handling and shipping as outlined in the protocol and within institutional/KUMC policy.
Ensure adequate study supplies are being maintained. Track study expenditures and submit reimbursement requests for study equipment supplies and study participants.
Prepare documentation and participate in study monitoring visits reviews and audits. Provide written and verbal reports to Principal Investigator and Project Manager as required.
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.
Work closely with the Research Institute and Human Research Protection Program and have a working knowledge of KUMC policies and procedures.
Attend continuing education research and training seminars as requested by manager.
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: Associates degree plus two years related work experience OR an equivalent combination of relevant postsecondary education and work experience that equals at least 4 years.
Work Experience:
Experience with regulations governing clinical research (CFR GCP HIPAA).
Experience with statutes and guidelines relevant to regulatory affairs in clinical research.
Experience study budgets contracts and grant applications.
Preferred Qualifications
Education: Bachelors degree.
Certification: Research certification such as Certified Clinical Research Coordinator (CCRC) or certification eligible Certified Clinical Research Professional (CCRP) or certification eligible Collaborative Institutional Training Initiative (CITI) training certification or certification eligible.
Skills:
Communication skills including written verbal and presentation.
Organizational skills.
Required Documents:
Resume/CV
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. Employerpaid life insurance longterm 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
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