Regulatory Coordinator - Cancer Center

This job was posted by https://www.kansasworks.com : For more information, please see: https://www.kansasworks.com/jobs/13679707 Regulatory Coordinator - Cancer Center Department: SOM KC Cancer Center Clinical Trials ----- Regulatory Affairs Position Title: Regulatory Coordinator - Cancer Center Job Family Group: Professional Staff Job Description Summary: The Regulatory Coordinator is responsible for performing study-specific regulatory and safety reporting across multiple studies. This will be accomplished by: assuring the research is compliant with applicable federal, state or international requirements, while adhering to policies of The University of Kansas Medical Center. This position will be the assigned contact for study-start up activities including IRB/Ancillary committee submissions, and maintenances of regulatory records throughout the life of an assigned protocol. The University of Kansas Cancer Center is the region's only National Cancer Institute-designated comprehensive cancer center where patients gain access to the most promising therapies, cutting-edge clinical trials and world class research. Job Description: Job Duties Outlined: - Prepare and submit all regulatory documents including to the Institutional Review Board, collaborate with team members to ensure regulatory documents are complete and accurate. - Process, route, and track regulatory documents for study start-up. - Maintain trial master file and/or regulatory binder. - Maintain study files for team credentials (GCP Training, CV, Medical License). - Provide assistance to study monitors during routine monitor visits or audits - Update protocol-specific systems with complete and accurate protocol and study information. - Update regulatory documents as assigned: - Adding/removing study team members from regulatory documents - Printing, sorting, and filing documents - Updating templates" - Work closely with investigators, study personnel, and sponsors on relevant regulatory and/or safety concerns. - Ensure activities are conducted in a professional and ethical manner, and in accordance with KUMC Policies and applicable local, state and federal laws and regulations. - Ensure coordination of area work with other areas of KUMC to ensure integration and support of KUMC goals and objectives. - May participate in relevant committees, task force, or other similar activities. - Maintain confidentiality of medical center, employee, and patient information. Handle sensitive data with discretion and in accordance with KUMC policies and legal requirements. 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 may be eligible for a hybrid work schedule after 6 months. Incumbent will work remotely and on campus based on a set departmental schedule based on management approval and must reside in the greater Kansas City metropolitan area. Required Qualifications Work Experience: - Four (4) years of work experience in healthcare or research setting. Education may be substituted for experience on a year for year basis. - Work experience in an environment requiring an understanding of regulations governing clinical research (CFR, GCP, HIPAA) and statutes and guidelines relevant to regulatory affairs in clinical research. - Expe ience with medical terminology and concepts. - Experience with Microsoft Office Suite (Word, Excel, Outlook, PowerPoint). Preferred Qualifications Education: - Bachelor's degree in relevant field like health sciences, biology, nursing, or a related field. Skills: - Initiative - Organization - Detail-Oriented - Interpersonal - Multitasking - Communication - Analytical - Problem-solving - Time management 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 gene