Clinical Research Coordinator - Cancer Center

University of Kansas Medical Center • Kansas City, KS • 3h ago

This job was posted by https://www.kansasworks.com : For more information, please see: https://www.kansasworks.com/jobs/13354810

rClinical Research Coordinator - Cancer Center

Department:

SOM KC Cancer Center Clinical Trials

Clinical Trials, Clinical Trials Operations

Position Title:

Clinical Research Coordinator - Cancer Center

Job Family Group:

Professional Staff

Job 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 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. The Clinical Research Coordinator monitors participants\' progress including documenting and reporting adverse events and participates in periodic quality assurance audits of protocols.

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, cutting-edge clinical trials and world class research.

Job Description:

Job Duties Outlined:

Under the direction of the principal investigator, 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.

Work Environment:

This position will be 100% onsite due to the fact this is a patient facing role.

Required Qualifications

Education:

Associate degree plus two years related work experience OR an

equivalent combination of relevant post-secondary education and work experience that equals at least 4 years.

Education may be substituted for experience on a year for year

basis.

Work Experience:

Two years related work experience plus Associate\'s degree OR an

equivalent combination of relevant post-secondary education and work experience that equals at least 4 years.

Experience with regulations governing clinical research (CFR, GCP,

HIPAA).

Experience with statutes and guidelines relevant to regulatory

affairs in clinical research.

Experience with study budgets, contracts and grant applications.

Preferred Qualifications

Education:

Bachelor\'s degree in relevant field.

Certifications/Licenses: Research certification such as:

Certified Clinical Research Coordinator (CCRC) or certification

eligible

Certified Clinical Research Professional (CCRP) or certification

eligible

Skills

Communication.

Organization.

Presentation skills.

Interpersonal skills.

Time management.

Multi-tasking.

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 em

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