Manager of Research Blood Cancer

Research Manager The Research Manager is responsible for overall leadership and direction of the facility's research program, including fiscal management, study and site operations, and oversight of day-to-day operations. Responsibilities Oversee clinical trial-related activities by the research staff to ensure completeness and accuracy and adherence to federal and state guidelines. Problem solve clinical situations with the research staff and the management team as they arise. Assess the organizational processes associated with trial execution and identify ways to improve and streamline internal procedures. Plan, facilitate, and present trial management issues and data status updates at internal and external meetings. Provide oversight, leadership, and direction in the management and execution of trials. Assess quality of data and performance of clinical trials and develop action plans to address performance gaps. Manage, monitor, and operate within approved budget. Review all program billing outcomes and work with billing staff and Sarah Cannon to address issues impacting financial outcomes and patient billing experience. Work to ensure successful implementation of the EMR and optimize clinic processes related to OncoEMR implementation to support clinic outcomes and patient experience. Promote communication and accountability between staff and physicians. Monitor billing colleagues and services, provide financial reports and complete financial analysis to determine areas for improvement in financial outcomes. Maintain competency and enhance professional growth and development through continuing education, conferences, and seminars. Enhance operational effectiveness, emphasizing cost containment without jeopardizing innovation or quality of care. Oversee all aspects of patient treatment associated with trial execution, including enrollment, patient consent, lab work, data entry, and drug storage and distribution. Keep the executive team abreast of issues, progress, and risks related to trial operations and the overall clinic and meet frequently with all investigators. Assist in developing and executing internal and external strategies. Recruit, hire, train, develop, and terminate colleagues, as necessary. Qualifications Bachelor's Degree is required. Knowledge of FDA guidelines and GCP. Must be able to read, understand, and comply with research protocols. Experience using clinical trial databases, electronic data capture, MS Access, and MS Excel. Oncology experience preferred. Experience in clinical trials research. We are an equal opportunity employer and value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status. #J-18808-Ljbffr McKesson Corporation