Screening and Eligibility Manager - Cancer Center

This job was posted by https://www.kansasworks.com : For more information, please see: https://www.kansasworks.com/jobs/13703643 Screening and Eligibility Manager - Cancer Center Department: SOM KC Cancer Center Clinical Trials ----- Clinical Trials Trial Management Services Position Title: Screening and Eligibility Manager - Cancer Center Job Family Group: Professional Staff Job Description Summary: The Screening and Eligibility Manager is responsible for coordinating referrals, prescreening, and eligibility review for clinical trials across different disease working groups within The University of Kansas Cancer Center. The University of Kansas Cancer Center (KUCC) 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: - Attend study specific training, including but not limited to, site initiation visits, kick off meetings, investigator meetings (as deemed appropriate by leadership) for new clinical trials. - Present protocol summaries and eligibility requirements at disease-specific workgroup meetings, as assigned. - Recruit/screen for study patients and identify inclusion/exclusion criteria. This includes proactively obtaining medical records for potential trial patients and pre-screen patients for potential clinical trials throughout program trial portfolio. - Coordinate with study teams to monitor clinical trial slot and cohort availability to support patient prescreening and referrals. - Provide regular reports to leadership on prescreening activities, eligibility outcomes, and patient additions to waitlists. - Facilitate timely communication and handoff of potentially eligible patients to the appropriate clinical research teams for consenting and screening. - Utilize Epic/Beacon, and any other systems required for scheduling, screening and treating new clinical trial patients. - Assist leadership in the development of Standard Operating Procedures and Working Practice Guidelines related to clinical trial referral process, prescreening, and eligibility review. - Document all communication (i.e. telephone and other) with patients per University and Health System policies. - Participate in team meetings and collaborate with study team members to review referral, prescreening, and eligibility updates. - Participate in protocol feasibility discussions and internal committees as requested by leadership, providing input on prescreening and eligibility requirements for new clinical trials. - Provide prescreening and eligibility support across clinical trial programs as operational needs require. 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: Certifications: - Certified Clinical Research Coordinator (CCRC) or - Certified Clinical Research Professional (CCRP) or {=html} - Other equivalent recognized clinical research certification. Work Experience: - 8 years of clinical research experience. Education may be substituted for experience on a year for year basis. {=html} - Experience interpreting clinical trial protocols and eligibility criteria. - Experience with Electronic Medical Record charting. - Experience adhering to guidelines regarding transparent and honest reporting of confidential and sensitive patient information. - Knowledge of clinical research databases and software. - Experience with MS/Office - Proficiency in medical terminology. Preferred Qualifications: Work Experience: - Previous oncology clinical research experience highly preferred. Skills: - Oral and written communication. - Attention to detail. - Organization. - Computer skills. - Project management. - Time management. - Multitasking. {=html} - Work independently and collaboratively. {=html} - Critical thinking and problem-solving. 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 p