Kansas Works Jobs

Kansas Works Logo

Job Information

University of Kansas Medical Center Clinical Research Coordinator in Kansas City, Kansas

This job was posted by https://www.kansasworks.com : For more information, please see: https://www.kansasworks.com/ada/r/jobs/11299011 Clinical Research CoordinatorDepartment:SOM KC Cancer Center Clinical Trials-----Clinical Trials Clinical OperationsPosition Title:Clinical Research CoordinatorJob Family Group:Professional StaffJob Description Summary:The Clinical Research Coordinator 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.The University of Kansas Cancer Center is the region's only National Cancer Institute-designated cancer center where patients gain access to the most promising therapies, cutting-edge clinical trials and world class research.Join our clinical trials team where you can make a difference!The starting salary is between the minimum and midpoint of the salary range listed.Job Description:Required Qualifications: Education: Associate's 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. Experience: Basic understanding of regulations governing clinical research (CFR, GCP, HIPAA). Solid understanding of statutes and guidelines relevant to regulatory affairs in clinical research. Knowledgeable of study budgets, contracts and grant applications. Skills: Excellent communication, writing, organizational and presentation skills. Ability to effectively interact with multidisciplinary teams including physicians, administrative staff. Ability to recognize competing priorities and deadlines and seek guidance in management of these where needed. Willingness to seek research certifications to further skills in the position.Preferred Qualifications: Research certification preferred such as Socra certification or certification eligible: 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: Ability to read, speak and write Spanish preferred.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 documenta tion 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. Perform other duties as assigned.Required Documents:Must provide the following: Resume & Cover LetterEmployee Type:RegularTime Type:Full timePay Rate Type:SalaryPay Grade:A12Pay Range:Minimum56721Midpoint72562Maximum87892Application Instructions:To learn more and apply online, please visit https://apptrkr.com/2018485 or go to https://jobs.kumc.edu/ and search for position number JR000680.Applications must be submitted directly through the KU Medical Center website to be considered for this position. Any applications submitted via email or this website will NOT be reviewed or considered.About KU Medical Center:The University of Kansas Medical Center's mission is to educate exceptional health care professionals through a full range of undergraduate, graduate, professional, postdoctoral and continuing education programs in the schools of Medicine, Nursing and Health Professions. KU Medical Center also advances the health sciences through world-class research programs; provides compassionate and state-of-the-art patient care in an academi