Clinical Research Coordinator II (DOM Bayview Infectious Diseases)
Core
Administratively coordinates complex pharmaceutical-sponsored clinical trials and NIH-funded research protocols for adults with HIV, hepatitis, COVID, and other infectious diseases.
Role type
Clinical Research Coordinator II
Builds
Clinical research studies for Johns Hopkins University
Domain
Infectious diseases clinical research
Deliverable
client delivery
Required skills
Protocol implementation, participant recruitment, informed consent administration, data entry and organization, regulatory documentation management, budget oversight, literature search and analysis, clinical sample procurement coordination
Preferred skills
None stated
Technologies
Clinical computer systems, data collection systems
Responsibilities
Coordinate all activities of complex clinical research studies to ensure protocol adherence; Participate in clinical study start-up meetings; Explain study background and rationale to potential and current participants; Contribute to the development of recruitment strategies; Independently conduct the consenting process; Schedule participants for required activities and resolve conflicts; Serve as liaison to study participants; Assist with the setup of data collection systems; Assist with preparation of submissions to the Institutional Review Board (IRB); Track and maintain regulatory and clinical care documentation; Oversee budget expenditures for study operations; Coordinate site initiation visits for multisite studies