Clinical Research Coordinator - DOM Infectious Disease

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 integrityManage participant recruitment, screening, informed consent, scheduling, and ongoing communicationServe as liaison between study participants, Principal Investigators, sponsors, and the IRBAssist with IRB submissions, amendments, continuing reviews, and regulatory correspondenceOversee study data entry, documentation, and operational budget trackingSupport site initiation visits and collaborate across multisite study operationsCoordinate infusion/injection-based study workflows and medication administration processes associated with clinical trials as experience permitsEnsure accurate maintenance of study documentation and adherence to institutional and federal research guidelinesSkill Set Requirements:

Relevant undergraduate or professional experience supporting human subjects research3–5 years of Clinical Research Coordinator or related clinical research experienceStrong understanding of clinical trial operations, participant management, and regulatory processesAbility to work independently and manage complex study workflows with minimal oversightFamiliarity with IRB processes and regulatory submissions in complex clinical studiesExperience working within an academic medical center or multisite research environmentBachelor’s degree in a related field


Preferred Qualifications:

Prior experience supporting infectious disease, GI, hepatology, HBV, HIV, or HDV research studiesExperience with infusion/injection-based clinical trials and medication administration workflows