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Sr. Clinical Research Coordinator (Psychiatry and Behavioral Sciences) - #Staff

Johns Hopkins University

Baltimore, MDFull-time$42–74K/yrSeen 2 days agoSeen in employer's feed 2 days ago

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At a glance

Compensation
$42–74K/yr
Location
Baltimore, MD
Schedule
Full-time
Work Authorization
Not specified

Olive focuses on jobs in the United States, including remote roles you can work from there.

Job overview

Johns Hopkins University’s Bayview Geriatric & Neuropsychiatry seeks a Senior Clinical Research Coordinator to oversee complex clinical research studies, make independent decisions affecting study conduct, and contribute to goal setting, implementation plans, budgets, communications, and data systems. The role includes coordinating participant recruitment and assessments, managing study data and regulatory submissions, and overseeing blood collection and shipment to a national repository.

Skills & qualifications

RequiredNice to have

Skills

Budget Management, nice to haveParticipant Recruitment, nice to haveClinical Study Design, nice to haveClinical Trial Management System, nice to haveData Management and Analysis, nice to haveData Collection and Reporting, nice to haveGood Clinical Practices, nice to haveInterpersonal Skills, nice to haveProject Management, nice to haveRegulatory Compliance, nice to haveReport Writing, nice to haveTask Coordination, nice to have

Qualifications

Bachelor's Degree in Related Field, requiredThree Years Related Experience, requiredMaster's Degree in Related Field, nice to have

Full job description

Researchers at Johns Hopkins University conduct clinical trials and clinical studies to discover new ways to prevent and treat diseases and other health problems. Bayview Geriatric & Neuropsychiatry is seeking a Sr. Clinical Research Coordinator oversees the day-to-day activities of a single complex study (e.g., in-patient study, translational research involving clinics and labs, participant accrual at multiple sites, study for which Hopkins is a coordinating center) or multiple clinical research studies and makes independent decisions that impact the conduct of the research. Assists in goal setting and creating implementation plans. Contributes to budget formulation, communications, and data systems.

Specific Duties & Responsibilities

  • Assist Principal Investigator or more senior research staff to ensure operational feasibility of proposed protocol/study design.

  • Develop standard operating procedures and data collection forms from protocol(s).

  • Develop consent form(s) for clinical trials based on protocol(s).

  • Prepare materials for submission to IRB.

  • Contribute to work with commercial and/or government agency sponsors and recommend which group can commit to considering patient population, available resources, and cost of providing services.

  • Ensure compliance with all protocols, procedures, and applicable regulations.

  • Participate in developing the study budget.

  • Develop and oversee the implementation of recruitment strategy for participants for one or more assigned studies.

  • Set up a data collection system and ensure the validity of study data.

  • Organize and quality control study data

  • Perform self-audits and/or audit other sites.

  • Participate in study meetings and provide status updates and recommend changes to protocol operations based on results and goals.

  • Conduct literature searches to provide background information.

  • Abstract and index information based on knowledge of subject matter.

  • Other duties as assigned.

In addition to the duties described above

  • Oversee collection and shipping of blood to national repository.

  • Conduct comprehensive clinical and cognitive assessments of research participants in accordance with study protocols and standardized procedures.

Minimum Qualifications

  • Bachelor's Degree in a related field.

  • Three years 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.

Preferred Qualifications

  • Master's Degree in a related field.

  • Proficiency in coordination of tasks across multiple research teams.

Technical Skills & Expected Level of Proficiency

  • Budget Management - Developing

  • Clinical Research Participant Recruitment: -Developing

  • Clinical Study Design - Developing

  • Clinical Trial Management System - Developing

  • Data Management and Analysis - Developing

  • Data Collection and Reporting - Developing

  • Good Clinical Practices - Developing

  • Interpersonal Skills - Developing

  • Project Management - Developing

  • Regulatory Compliance - Developing

  • Report Writing - Developing

The core technical skills listed are most essential; additional technical skills may be required based on specific division or department needs.

Classified Title: Sr. Clinical Research Coordinator

Role/Level/Range: ACRP/03/MB

Starting Salary Range: $42,330 - $74,110 Annually ($51,000 targeted; Commensurate w/exp.)

Employee group: Full Time

Schedule: M-F 9am - 5pm

FLSA Status: Exempt

Location: Johns Hopkins Bayview

Department name: SOM Psy Bay BV Geriatric and Neuropsychi

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.

How this job compares

Set against the 619 open Clinical Research Coordinator jobs on Olive Jobs, counted November 13, 2026.

Pay
  • This posting$42–74K/yr
  • US median$56–76K/yr165 salary ranges

This range's midpoint, $58K, is 12% below the US median midpoint ($66K) — in the lowest quarter of Clinical Research Coordinator salary ranges across the US.

Openings
Olive Jobs lists 32 open Clinical Research Coordinator jobs in Maryland and 619 across the US. 2% of them nationwide are listed as remote or flexible.
Hiring the most in Maryland
Experience
This posting asks for at least 3 years of experience; Clinical Research Coordinator postings that state a minimum ask for 2 years at the median (421 postings).
Education
184 of the 619 open Clinical Research Coordinator jobs (30%) ask for a bachelor's degree or higher.

Counted across the open, public US postings on Olive Jobs on November 13, 2026. Figures based on too few postings are left out.

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