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Sr. Clinical Research Coordinator (Research Administration) - #Staff

Johns Hopkins University

Baltimore, MD · HybridJob$21.7–38/hrSeen 3w ago

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At a glance

Compensation
$21.7–38/hr
Location
Baltimore, MDHybrid
Work Authorization
Not specified

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Requirements

Credentials this posting asks for.

Bachelor's degree

Job overview

Johns Hopkins University seeks a Sr. Clinical Research Coordinator to oversee day-to-day activities of complex clinical studies, develop SOPs, consent forms, and data systems, ensure regulatory compliance, manage budgets and recruitment, and support IRB submissions while collaborating with investigators and sponsors.

Skills & qualifications

RequiredNice to have

Skills

Budget ManagementClinical Research Participant RecruitmentClinical Study DesignClinical Trial Management SystemData Management and AnalysisData Collection and ReportingGood Clinical PracticesInterpersonal SkillsProject ManagementRegulatory ComplianceReport Writing

Qualifications

Bachelor's Degree in Related FieldThree Years of Related ExperienceMaster's Degree in Related Field

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. We are 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.

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.

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 : $21.70 - $38.00 HRLY ($29,462 targeted; Commensurate w/exp.)

Employee group: Limited

Schedule : Monday - Friday (expected to average 28 or more per week)

FLSA Status: Exempt

Location : Hybrid/School of Nursing

Department name: Research Administration

Personnel area: School of Nursing

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.

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