We are seeking a **_Research Program Coordinator_** to join the Center of the Electrophysiology Clinical Trials. This program supports a variety of ongoing and future clinical research studies within the Division of Cardiology. The position is ideal for individuals starting their careers in clinical research or transitioning into the field, as training and mentorship will be provided. **Specific Duties & Responsibilities** + Assist in the coordination and oversight of clinical research studies in Electrophysiology, working collaboratively with the research team to ensure project success. + Recruit and coordinate research subjects according to study objectives. + Communicate study details and obtain informed consent (in-person or via telephone) with proper documentation in electronic medical records. + Schedule study follow-up visits and research-related tests within the study timeframe to minimize protocol deviations. + Monitor participants for protocol adherence and provide follow-up as needed. + Implement and maintain data collection and analysis systems, including management of subject binders, paper files, and electronic databases. + Organize and maintain study records according to regulatory guidelines, ensuring compliance with HIPAA and patient privacy statutes. + Assist with data collection, including conducting interviews and administering surveys. + Ensure study-related supplies and equipment are available and functional. + Prepare and submit research documents (e.g., protocols, amendments) to IRBs and other oversight bodies. + Maintain compliance with Good Clinical Practice (GCP), ICH guidelines, IRB requirements, and federal regulations. + Assist with study timelines to ensure tasks are completed on schedule. + Participate in team meetings and provide study updates. + Collaborate with internal and external partners to facilitate project execution. + Collect and enter data from medical records and questionnaires, ensuring accuracy. **Additional Knowledge, Skills, & Abilities** + Strong organizational, time management, and problem-solving skills. + Ability to work independently and prioritize multiple tasks. + Excellent interpersonal and communication skills for engaging with participants and team members. + Attention to detail and adherence to research best practices and regulatory compliance. + Note: Training will be provided for tasks such as specimen handling, venipuncture, and laboratory procedures, as required. **Minimum Qualifications** + Bachelor's Degree in related discipline. + Additional related experience may substitute for required education, to the extent permitted by the JHU equivalency formula. **Preferred Qualifications** + Interest in clinical research and cardiology, particularly Electrophysiology. + Experience with customer service or participant-facing roles. + Knowledge of medical terminology and clinical research processes. Classified Title: Research Program Coordinator Role/Level/Range: ACRO40/E/03/CD Starting Salary Range: $17.20 - $30.30 HRLY ($49,400 targeted; Commensurate w/exp.) Employee group: Full Time Schedule: M-F 8:30 am - 5:00 pm FLSA Status: Non-Exempt Location: School of Medicine Campus Department name: ​​​​​​​SOM DOM Cardiology Personnel area: School of Medicine The listed salary range represents the minimum and maximum Johns Hopkins University offers for this position, based on a good faith estimate at the time of posting. Actual compensation will vary depending on factors such as location, skills, experience, market conditions, education, and internal equity. Not all candidates will qualify for the highest salary in the range. Johns Hopkins provides a comprehensive benefits package supporting health, career, and retirement. Learn more: https://hr.jhu.edu/benefits-worklife/. Equal Opportunity Employer All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran. EEO is the Law https://www.eeoc.gov/sites/default/files/2023-06/22-088_EEOC_KnowYourRights6.12ScreenRdr.pdf