Residency Coordinator - Diagnostic Radiology GME - Full-time

14889
April 25, 2025

Job Description

Location: Chicago, Illinois Business Unit: Hospital: Rush University Medical Center Department: Diagnostic Radiology GME Work Type: Full Time (Total FTE between 0. 9 and 1. 0) Shift: Shift 1 Work Schedule: 8 Hr (8:00:00 AM - 4:30:00 PM) Rush offers exceptional rewards and benefits learn more at our Rush benefits page (https://www.rush.edu/rush-careers/employee-benefits). Pay Range: 23.12 - 36.41 Rush salaries are determined by many factors including, but not limited to, education, job-related experience and skills, as well as internal equity and industry specific market data. The pay range for each role reflects Rush’s anticipated wage or salary reasonably expected to be offered for the position. Offers may vary depending on the circumstances of each case. Summary: The Residency Coordinator will aid and represent the Residency Director for the program's house staff. The Residency Coordinator will assist the residency program application process, orientation, rotation support, rotation schedule, program administration, grant preparation, budget management, website, and attending and resident awards. Exemplifies the Rush mission, vision and values and acts in accordance with Rush policies and procedures. Other information: Required Job Qualifications: • Bachelor's degree. • 2 years of office management experience, or equivalent experience in administration and office management in an academic health care setting. • Excellent communication. • Good technical skills: Computer literacy (Word, Excel, ERAS, NRMP, et al). • Excellent problem-solving and decision-making skills. • Organizational expertise and attention to detail. • Professionalism in dealing with confidential information. Responsibilities: • Manages and coordinates the entire process of recruitment including pre-recruitment, recruitment, and post-recruitment activities. • Uses selection criteria to choose applications for review by the residency director or Admissions Committee. • Utilizes ERAS to review applications. • Communicates with potential applicants, applicants and matched incoming housestaff. • Offers and confirms interview dates for residency candidates. • Provides applicants with information about the program, interview process, transportation and accommodations. • Compiles a list of attending physician interviewers. • Organizes orientation schedule including events at Rush and affiliated institutions. • Assists new residents with "settling in to" the program and Chicago including preparing packet with information about housing, transportation and utilities. Fields questions to ease transition. • Completes CA-MED forms to indicate acceptance into program for licensure packet. • Provides correct Housestaff Data Sheets in timely fashion to GME for input. • Collects email addresses for all incoming and is the liaison for distributing GME and program-related information. • Informs GME of program's orientation dates and locations. • Arranges for any BLS and ACLS classes necessary for incoming housestaff. • Arranges for program-specific needs such as scrubs, electronic swipe badges, mailboxes, etc. • Schedules conference rooms for seminars and conferences and audiovisual aids. • Arranges food for selected conferences. • Develops, coordinates and maintains materials for course directors to evaluate resident trainees. • Develops and maintains system for soliciting and receiving resident evaluations of rotations and faculty, and providing feedback to faculty on their teaching skills. • Tracks electives for housestaff and may facilitate any off-site electives and required documents. • Compiles and tabulates data for surveys, questionnaires, census reports, accreditation reports, WebADS, ERAS, ERMA, annual reports, duty hours monitoring and attestations, case log/stat data, residency competencies toolbox. • Keep program director on target with dates and deadlines, meeting coordination and reports for accreditation, the appropriate Board requirements, GMEC Internal Reviews and other GME needs. • Serves as the liaison between the trainees and the program director and keeps the communication lines active and open. • Makes all necessary arrangements for the Site Visitor (welcome, scheduling, agenda, food, room set-up, document preparation and other needs). • Maintains databases and statistics required by funding agencies including resident and graduate biographical information, career choice, practice location and practice demographics. • Assists residency director with preparation of grant applications. • Proctors In-Service training exams. • Solicits, creates and submits website updates to ensure information posted about the training program is accurate, complete, and up-to-date, coordinating with GME and Rush Marketing Communications and Information Services. Provides follow-up to ensure completion. • May take the Content Management Class and become the content manager responsible for all the writing and editing. • May be responsible for the photographs submitted to upload to the program website. • Formulates ballots for attending teaching and resident awards. Distributes ballots as requested for each award. • Tabulates ballots. • Encourages all award recipients to attend graduation banquet. • Prepares or orders certificate awards. • Provides secretarial support to the program director and/or associate program director and house officers including receiving telephone calls, taking messages, mail receipt and distribution, email notifications, and preparing and submitting letters of recommendation and verifications. • Responsible for verifying the program's group email mnemonic and utilizes it for distribution of information to housestaff from program. • Composes, prepares and distributes correspondence, agendas, reports and schedules. • Transcribes letters, dictations, reports, manuscripts, slides, etc. for program and/or associate director. Rush is an equal opportunity employer. We evaluate qualified applicants without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status, and other legally protected characteristics.

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Required Job Qualifications: · Bachelor’s degree required. · At least 2 years of supervisory and regulatory experience required. · At least seven years of experience in the academic or pharmaceutical clinical research environment required. · Relevant certification as a Certified Clinical Research Professionals (CCRP), Certified Clinical Research Associate (CCRA), Certified Clinical Research Coordinator (CCRC), or Certified IRB Professional (CIP). · Ability to multitask and manage several projects in parallel, paying attention to detail. · Strong knowledge of the Code of Federal Regulations pertaining to Human Subject Protections, including 45CFR46, 21CFR50, and 56, Good Clinical Practice, the Declaration of Helsinki, the Belmont Report, and HIPAA required. · Demonstrated expertise in clinical research methodologies, regulations, and guidelines. · Must be able to direct a team effectively while also working independently with minimal supervision, with excellent written and oral communication skills. · Proficient using the Microsoft Office suite and other computer programs. Preferred Job Qualifications: · Master’s degree preferred. Responsibilities: · Manages and develops a team of regulatory coordinators, but not limited to supervisor of the research team, clinical research coordinators, research nurses, and lab staff. · Leads regular, timely meetings to track progress of study regulatory activities, including study start-up, maintenance, close-out activities; and provides direct feedback to team members (regulatory documentation completion; IRB (local and central) submission preparation and requirements). o Manage the daily operations of clinical research studies by coordinating various essential activities. This includes the meticulous design of study protocols, ensuring they adhere to regulatory standards and scientific rigor. Oversee the systematic collection of data from participants, implementing robust methodologies to guarantee accuracy and integrity. Additionally, analyze the gathered data using advanced statistical techniques to draw meaningful conclusions and insights, ultimately contributing to the advancement of medical knowledge and improving patient outcomes. · Initiates start-up and training tasks for new study staff; registers for trainings (EPIC, CITI, ONCORE, Rush Internal Review Board (IRB) portal, Rush mandatory safety training); creates yearly goals for new staff and others as delegated by the Research Manager; completes the 30- and 90-day evaluations for new staff; sets up meetings often during the initial training period to ensure proper procedures and policies are learned; completes mid and yearly performance reviews. · Works directly with the Finance Director and/or the Research Manager to help solve problems when issues arise; assists the Research Manager with overall disciplinary functions for all study staff; leads staff meetings to communicate upcoming regulatory issues, special events, and other topics relevant to the current research projects. · Monitors and audits research staff work to ensure clinical research activities are conducted in accordance with ICH GCP guidelines, FDA regulations and guidance documents; creates and updates Rush’s SOPs, departmental SOPs, and applicable federal and state regulations and guidelines; identifies regulatory and compliance issues; and provides guidance, direction, and/or training when necessary to reduce or eliminate errors in the performance of clinical trials. · Attends meetings with leadership to stay current on new and updated information shared by entities that function within Rush (regulatory, compliance, revenue cycle, sponsor invoicing, legal, 3rd party vendors, etc.), and outside entities (FDA, pharmaceutical companies, foundations, etc.) that communicate new policies, processes, or guidelines; shares findings to study staff and other members of the research team, as needed. · Supports Principal Investigators (PIs) with submissions for investigational new drug (IND), investigational device exemption (IDE), and/or biologics applications to the FDA; and coordinates regulatory activities for Rush-led multi-site research protocols including management of ClinicalTrials.gov web pages. · Maintain documentation of staff credentials and qualifications (e.g., CVs, licenses, GCP, Certificates) and facilitate updates and/or renewal as required. · Directs the preparation for audits and local monitoring visits; acts as the regulatory representative for all external and internal audits; prepares study staff in all aspects of audits: internal audits, sponsor audits, and FDA inspections of research studies; clinical trial processes: site qualification visits, (SQV), site initiation visits (SIV), interim monitoring visits (IMV), and close-out visits. · Tracks, audits, and reports about submissions to ancillary committees such as Protocol Review and Monitoring Committee, Radiation Safety Committee, Investigational Pharmacy, and Institutional Biosafety Committee. · Serves as a backup to the Research Manager as needed; assumes all duties of a regulatory coordinator, and other duties as needed; orders supply for clinic, research, and office. · Other duties as assigned. Rush is an equal opportunity employer. We evaluate qualified applicants without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status, and other legally protected characteristics.