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We are seeking a **_Research Protocol Specialist_** who will provide administrative support for research centers, research review, and clinical trial committees. The Specialist will ensure that protocols and associated documents are processed, tracked, and maintained in compliance with institutional, regulatory, and sponsor requirements.

Specific Duties & Responsibilities

+ Coordinate the submission, tracking, and scheduling of research protocols for internal review.

+ Review submissions for completeness and accuracy; manage protocol amendments and annual updates.

+ Maintain databases and tracking systems with up-to-date protocol status and outcome data.

+ Prepare and distribute review outcomes and communications to investigators and study staff.

+ Attend and document meetings related to protocol and safety reviews; track issues and resolutions.

+ Upload, organize, and maintain study-related documents in internal systems or libraries.

+ Enter study data into required institutional or sponsor registration systems.

+ Assist with protocol development, consent document drafting, and preparation of regulatory submissions.

+ Coordinate the research protocol documents and manage pre-written documents through development.

+ Coordinate research study logistics and support regulatory and operational approval processes.

+ Ensure compliance with institutional, sponsor, and federal requirements for research protocols.

+ Communicate with research sites, sponsors, and oversight bodies regarding study progress and requirements.

+ Coordinate projects, timelines, and priorities independently or as part of a team.

+ Participate in the development of standard operating procedures and internal workflows.

+ Support staff training as needed.

+ Other duties as assigned.

Minimum Qualifications

+ High school diploma or graduation equivalent.

+ Three years 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.

Preferred Qualifications

+ Bachelor’s Degree.

+ Experience in a clinical research environment.

Classified Title: Research Protocol Specialist

Role/Level/Range: ATO 40/E/03/OE

Starting Salary Range: $18.20 - $33.90 HRLY ($20-22/hour targeted; Commensurate w/exp.)

Employee group: Full Time

Schedule: Mon - Fri - 8:30a - 5p

FLSA Status: Non-Exempt

Department name: SOM Onc Clinical Research Office

Personnel area: School of Medicine

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.