Job Title: Clinical Research Coordinator - DOM Infectious Disease
Contract Length: 6 month with probability of extensions
Location: Baltimore, MD
Hours: 40/week, 9-5pm EST
Start Date: July 6, 2026
Job Description:
The Department of Medicine – Infectious Disease team at Johns Hopkins University School of Medicine is seeking an experienced Clinical Research Coordinator to provide interim coverage and assist the research team with the conduct of pharmaceutical-sponsored clinical trials, long-term NIH-funded or other investigator-initiated research protocols examining the treatment and progression of disease in adults with HIV, hepatitis, COVID and other infectious diseases. This role will support hepatitis-focused clinical research studies (HBV, HIV, HDV) and will be heavily involved in clinical trial coordination, participant communication, study operations, and regulatory support. The ideal candidate is a seasoned CRC capable of operating independently with minimal oversight in a complex academic research environment.
Responsibilities:
- Coordinate all activities related to clinical research studies to ensure protocol adherence, regulatory compliance, and data integrity
- Manage participant recruitment, screening, informed consent, scheduling, and ongoing communication
- Serve as liaison between study participants, Principal Investigators, sponsors, and the IRB
- Assist with IRB submissions, amendments, continuing reviews, and regulatory correspondence
- Oversee study data entry, documentation, and operational budget tracking
- Support site initiation visits and collaborate across multisite study operations
- Coordinate infusion/injection-based study workflows and medication administration processes associated with clinical trials as experience permits
- Ensure accurate maintenance of study documentation and adherence to institutional and federal research guidelines
Skill Set Requirements:
- Relevant undergraduate or professional experience supporting human subjects research
- 3–5 years of Clinical Research Coordinator or related clinical research experience
- Strong understanding of clinical trial operations, participant management, and regulatory processes
- Ability to work independently and manage complex study workflows with minimal oversight
- Familiarity with IRB processes and regulatory submissions in complex clinical studies
- Experience working within an academic medical center or multisite research environment
- Bachelor’s degree in a related field
Preferred Qualifications:
- Prior experience supporting infectious disease, GI, hepatology, HBV, HIV, or HDV research studies
- Experience with infusion/injection-based clinical trials and medication administration workflows