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  3. Clinical Research Assistant II (Oncology)
JH

Clinical Research Assistant II (Oncology)

Johns Hopkins University·Baltimore, Maryland

$16 - $26/hr·Full Time·Hybrid·0-2 yrs·Posted 29 days ago
Practice for this role

About the role

The role involves implementing clinical research protocols by recruiting participants and coordinating study activities. Additionally, the assistant performs administrative tasks, manages data entry, and serves as a liaison with the IRB.

Researchers at Johns Hopkins University conduct clinical trials and clinical studies to discover new ways to prevent and treat diseases and other health problems. We are seeking a Clinical Research Assistant II who will support the research team by implementing steps and processes of a clinical research protocol. The position will perform both administrative tasks related to day-to-day clinical research operations, and protocol-related duties requiring an understanding of research procedures.

Specific

Duties & Responsibilities

Collect study data by recruiting and coordinating activities of study participants. Utilize a basic understanding of the clinical study background and rationale to explain. the study to potential and current participants. Assist in developing recruitment strategy for one or more studies. Implement a variety of techniques for recruitment, e.g., print and web based. advertisements, contact referring physicians, participate in community events, etc. Set up tools and procedures for data collection and study processes. Perform data entry and organize data in approved systems. Serve as liaison between study team and IRB for routine administrative matters. Prepare routine reports related to study accrual, study trends, efficiency-related issues. Contact participants to confirm, schedule, and retain. Other duties as assigned.

Minimum Qualifications

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

Classified Title

  • Clinical
  • Research
  • Assistant
  • II
  • Role/Level/Range: ACRO37.5/02/CC Starting

Salary Range

$15.70 - $26.25 HRLY ($21.00/hour targeted; Commensurate w/exp.) Employee group: Full Time Schedule: Mon - Fri / 8:30a - 5p FLSA Status: Non-Exempt Location: Hybrid/School of Medicine Campus Department name: SOM Onc Urologic Oncology Personnel area: School of Medicine Read more

Requirements

A high school diploma or equivalent is required along with one year of related experience. Additional education or experience may be substituted according to the JHU equivalency formula.

  • high school
  • Data Entry
  • Report Preparation
  • Data Collection
  • Clinical Research
  • Patient Scheduling
  • Participant Recruitment
  • Clinical Trial Coordination
  • IRB Liaison

Posting details

Employment type
Full Time
Work arrangement
Hybrid
Experience
0-2 yrs
Salary
$16 - $26/hr
Location
Baltimore, Maryland
Posted
Jun 29, 2026
Application
Employer website
JH

Hiring organization

Johns Hopkins University

The Johns Hopkins University was the first university in the Western Hemisphere based on the European research institution, with a mission both to teach and to advance human knowledge through discovery. Its establishment revolutionized U.S. higher education. Today, Johns Hopkins...

Salary listed on 134 jobs
IndustryEducation Administration Programs
TypeEducational
Size2-10 employees
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Market context

Oncology research support in Maryland

Clinical Research Assistant II roles in oncology are often tied to active study enrollment, data collection, and regulatory support at cancer centers and academic hospitals in Maryland. Competition can be strong because employers often look for candidates who can balance patient-facing coordination, accurate documentation, and familiarity with research protocols; this listing’s requirements and benefits are AI-summarized from the original job description, which can save you time comparing details. Before applying, review the protocol language and be ready to show experience with clinical records, scheduling, or research compliance.

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