MOBERLY DIALYSIS CLINIC Clinical Research Coordinator in Kansas City, Missouri
Overview Founded in 1971, Company . DCI remains the nation s largest non-profit Company provider. With a team of approximately 5,000 talented and caring employees serving across the United States, DCI provides care to nearly 15,000 patients on Company and 3,500 patients with chronic kidney disease. We offer a variety of services including in-center hemodialysis, home hemodialysis, and peritoneal Company PD. Each position within DCI, from billers to administrators to nursing staff, contributes toward the goal of providing excellent patient care. Our staff has helped DCI achieve the lowest mortality and hospitalization rates among large Company providers for the past 13 years in a row. Clinical Research Coordinators provide support, coordination, and leadership for drug/device studies that may involve industry-sponsored Phase I, II, III, and IV clinical trials; government-funded clinical research, and investigator-initiated clinical research collectively referred to as clinical research involving human subjects . Responsibilities Ensure compliance with study protocols in order to provide consistent and quality data. Recruit and screen study participants, schedule clinical treatment and follow-up care, and facilitate patients' continued participation. Prepare documentation for submission for review by the Institutional Review Board IRB. Ensure smooth, accurate progress of clinical studies from the planning and approval stages through study completion and post-study closure. Perform detailed medical chart review and patient interview to ensure patient qualifies to be enrolled in the study. Manage informed consent process and ensure confidentiality practices are consistent with regulatory and study guidelines. Log and inform Principle Investigator PI of any possible adverse reactions or serious adverse events in a timely manner. Maintain study logs, IRB forms and Regulatory Binders for each clinical trial. Participate in routine monitoring visits from Sponsor and/or FDA audits. Conduct clinical trials in 2 or more outpatient Company units as needed. Travel overnight for Investigator Meetings as required. Qualifications Required-LPN or RN in good standing with a minimum of 1 year of full time experience coordinating clinical trials. Preferred-RN with at least 2 years of experience OR an individual with 5 years experience conducting clinical trials. CPR certified Reliable transportation, a valid driver s license, auto insurance, and be willing to travel to multiple DCI clinics within a given territory. DCI is a federal contractor and an Equal Opportunity/Affirmative Action Employer-Veterans/Individuals with Disabilities. If you are having difficulty using the online application system or would like to request other accommodations or application methods, please contact Doug Patterson at A or 615-327-3061. Once a request has been made, DCI will initiate a discussion with you about your needs and whether an accommodation can be provided. DCI is committed to providing such accommodations where possible. For more information about equal opportunity please see: company's website ; company's website ; company's website ; and company's website . ID 2018-8389 # of Openings 1 Address 6530 Troost Ave Category NursingDCI is an Equal Opportunity Employer/AA VEVRAA Federal ContractorEmployer's Job# 5B2DF48C9F7249E7A44FD634FA5AB639Please visit job URL for more information about this opening and to view EOE statement.