Clinical Research Site Manager, Neurology

JHU EEHPC

. Oversee site-level execution of large, multicenter clinical trials across a national network of collaborating clinical sites .

Posted 9/22/2026full-timeRemote • Maryland • United StatesMid-LevelSenior💰 $57,195 - $100,040 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in managing multicenter clinical trials, ensuring compliance with regulatory standards, and driving site performance through effective communication and resource management. Proficient in analytical skills and project management to deliver high-quality research outcomes.

Highest-signal resume keywords

Clinical Trials ManagementRegulatory ComplianceProject ManagementAnalytical SkillsInterpersonal Communication

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical Study DesignProcess ImprovementForecastingData AnalysisProtocol AdherenceSite AuditingQuality AssuranceEnrollment Performance TrackingResource-Readiness EvaluationSOP Development

Soft Skills

Attention to DetailOral CommunicationWritten CommunicationMentoringCollaboration

Industry Keywords

Clinical ResearchIRB SubmissionsInvestigational Product ComplianceMulticenter TrialsStakeholder EngagementQuality ReviewsTeleconferencesPerformance-Based Data InterpretationLean Management ProcessesOperational Improvements

About the role

Key responsibilities & impact

Oversee site-level execution of large, multicenter clinical trials across a national network of collaborating clinical sites
Lead site startup, feasibility assessments, resource-readiness evaluations, activation timelines, and centralized IRB/master agreement onboarding
Establish communication with clinical teams during identification, selection, preparation, and activation
Drive enrollment performance, track site-level metrics, identify underperforming sites, and develop customized remediation strategies
Manage investigator and site relationships; set expectations, assign deliverables, and hold sites accountable
Direct and monitor daily activities involving eligibility, randomization, protocol adherence, safety reporting, and investigational-product compliance
Ensure timely and accurate submissions to IRBs, sponsors, ethics committees, and master agreements
Conduct teleconferences, training broadcasts, and mentoring for coordinators and investigators
Provide support to quality assurance monitors
Manage site startup and performance plans, quality reviews, resource needs, escalations, and deadlines
Apply lean management processes to deliver trials on time, within budget, and to high-quality standards
Perform self-audits and site audits; recommend operational and protocol improvements
Track proposals and documentation through signature and approval processes
Use statistical, quantitative, explanatory, and predictive analysis to drive decisions
Help investigators interpret performance-based data
Facilitate meetings between project stakeholders and leadership
Maintain professional project documentation and deliverables
Develop SOPs and assist with study-site auditing and monitoring
Maintain knowledge of evolving clinical research technology and support innovation adoption
Serve as liaison between leadership and research communities
Perform other duties as assigned

Requirements

What you’ll need

Bachelor’s Degree in a related field
Five years of related experience delivering effective clinical research management solutions
Additional education may substitute for required experience, and additional related experience may substitute for required education beyond a high school diploma/graduation equivalent, subject to the JHU equivalency formula
Prior clinical research experience preferred
Intermediate analytical skills
Intermediate attention to detail
Intermediate clinical study design skills
Intermediate clinical trials knowledge
Intermediate forecasting skills
Intermediate interpersonal skills
Intermediate oral and written communication skills
Intermediate process improvement skills
Intermediate project management skills
Intermediate regulatory compliance skills
Successful candidates subject to a pre-employment background check
Faculty, staff, and students must receive the seasonal flu vaccine, subject to stated exceptions

Benefits

Comp & perks

Total rewards package supporting employees' health, life, career and retirement
Seasonal flu vaccine provided, with medical and religious exceptions
Required occupational-health vaccinations provided at no cost
Remote work arrangement
Monday–Friday schedule, 8:30 am–5:00 pm
Pre-employment accommodation support
Equal opportunity employment