Sr Clinical Research Coord

Job Summary The Sr. Clinical Research Coordinator is responsible for independently running and operating multiple research protocols in conjunction with the Principal Investigator and serves as a lead in the clinical research unit. Responsibilities Determines facility and supply needs required for set‑up and implementation of research protocols. Assists in identifying study related procedures for the project budget. Prepares for and is present for sponsor representative site visits. Provides regional leadership for assigned research. Be able to perform all of the duties of the Clinical Research Coordinator. Trains and/or may supervise Clinical Research Assistants and/or Clinical Research Coordinators. Assists with preparing for and conducting qualification, study initiation, interim monitoring, and close‑out visits at investigator sites in conjunction with the Clinical Research Manager. Qualifications 2+ years: Completion of a bachelor’s or associate degree from an accredited nursing program (RN) plus a minimum of three (3) years oncology research experience OR Completion of a bachelor’s degree in a related field plus a minimum of three (3) years oncology research experience. Must be a Certified Clinical Research Coordinator (CCRC-ACRP) or Certified Clinical Research Professional (CCRP-SoCRA). Previous coordinator experience. Oncology research experience. Ability to be detail oriented. Ability to be organized. Ability to communicate effectively both orally and in writing with all levels of the organization. Ability to effectively use interpersonal skills. Ability to independently manage time and priorities. Ability to navigate EMRs. Ability to travel between locations. Ability to use patient care skills to provide an exceptional experience. Ability to utilize Microsoft Office Suite. Demonstrates compliance with hospital standards, policies and procedures. Ability to communicate effectively both orally and in writing. #J-18808-Ljbffr Community Health Network