Clinical Research Coordinator II (DOM Bayview Infectious Diseases)

About the role

The Clinical Research Coordinator II assists the research team with the conduct of pharmaceutical-sponsored clinical trials, NIH-funded research protocols, and other investigator-initiated studies focusing on diseases such as HIV, hepatitis, and COVID.

Responsibilities

• Coordinate all activities of a complex clinical research study or multiple studies to ensure adherence to protocol and validity of findings.
• Participate in clinical study start-up meetings.
• Absorb and explain the study background and rationale to potential and current participants.
• Contribute to the development of the recruitment strategy for participants for one or more assigned studies.
• Implement various techniques for recruitment, including print and web-based advertisements, contacting referring physicians, participating in community events, etc.
• Independently conduct the consenting process or ensure consent is obtained from appropriate participants.
• Schedule participants for multiple required activities and resolve any schedule conflicts, ensuring timely participant tracking.
• Serve as a liaison to study participants.
• Assist with the setup of data collection systems and enter and organize data.
• Assist in coordinating study meetings and provide updates on protocol implementation status, making recommendations on operational issues.
• Assist with preparation of submissions to the Institutional Review Board (IRB) and liaise with the IRB on administrative matters.
• Track and maintain regulatory documentation and clinical care documentation to increase regulatory compliance.
• Conduct literature searches to provide background information, abstract, index, and analyze information.
• Obtain required samples and collaborate with internal and external entities for studies involving the procurement and processing of clinical samples.
• Oversee budget expenditures for study operations and ensure adequate study supplies are ordered and maintained.
• Train and/or oversee other non-exempt study staff.
• Coordinate site initiation visits for studies where Johns Hopkins is a participating site in a multisite study, is a single site for an investigator-initiated study, or is the coordinating center and a Hopkins PI is the lead or protocol chair.

Requirements

Minimum Qualifications:

• Bachelor's Degree in a related field.
• One year of related experience.

Additional education may substitute for required experience, and additional related experience may substitute for required education beyond high school diploma/graduation equivalent, to the extent permitted by the JHU equivalency formula.

Qualifications

• Classified Title: Clinical Research Coordinator II.
• Role/Level/Range: ACRO40/E/03/CE.
• Starting Salary Range: $41,080 - $73,528 Annually ($57,200 targeted; Commensurate w/exp.).
• Employee group: Full Time.
• Schedule: M-F 8:30am-5:00 pm.
• FLSA Status: Non-Exempt.