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 9/15/2026full-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 enrollment performance through effective communication and coordination with clinical teams. Proficient in project management, analytical skills, and process improvement to deliver high-quality research outcomes.

Highest-signal resume keywords

Clinical Trial ManagementRegulatory ComplianceProject ManagementAnalytical SkillsInterpersonal Communication

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical Study DesignFeasibility AssessmentResource-Readiness EvaluationStatistical AnalysisProtocol AdherenceEnrollment Performance MonitoringLean Management ProcessesSOP DevelopmentOperational ImprovementQuality Assurance Audits

Soft Skills

Decision-MakingAttention to DetailInterpersonal SkillsOral CommunicationWritten Communication

Industry Keywords

Clinical ResearchIRB ProcessesCompliance ProcessesInvestigational Product ComplianceSubject EligibilityRandomizationStakeholder LiaisonTraining ManagementRecruitment StrategiesContracting Processes

About the role

Key responsibilities & impact

Oversee site-level execution of large, multicenter clinical trials across a national network of collaborating clinical sites
Coordinate teams at other institutions and establish communication with clinical teams during identification, selection, preparation, and activation
Lead site start-up activities, feasibility assessments, resource-readiness evaluations, activation timelines, centralized IRB onboarding, and master-agreement processes
Drive enrollment performance and monitor monthly enrollment goals across clinical sites
Assist with IRB, sponsor, ethics committee, regulatory-document, contracting, and compliance processes
Oversee investigational-product compliance, safety-event reporting, subject eligibility, randomization, and protocol adherence
Identify recruitment problems and design customized remediation strategies with site teams
Conduct teleconferences, manage training broadcasts, and mentor coordinators and investigators
Manage investigator relationships, assign site tasks and deadlines, monitor daily site work, and escalate quality, functional, and timeline issues
Apply lean management processes to deliver trials on time, within budget, and to high-quality standards
Perform self-audits and clinical-site performance audits; recommend operational or protocol improvements
Track proposals and documentation through signature and approval processes
Use statistical and quantitative analysis, explanatory and predictive modeling, and fact-based management to drive decisions
Serve as liaison among project stakeholders, leadership, and research communities
Complete project documentation, develop SOPs, and assist with study-site auditing and monitoring
Maintain strong relationships and support adoption of evolving clinical research technologies

Requirements

What you’ll need

Bachelor’s Degree in a related field
Five years of related experience delivering effective clinical research management solutions
Demonstrated ability to independently manage and coordinate multiple external clinical sites
Advanced judgment and decision-making in high-stakes, time-sensitive research environments
Additional education may substitute for required experience, and additional related experience may substitute for required education beyond a high school diploma/graduation equivalent, as permitted by the JHU equivalency formula
Intermediate analytical skills
Intermediate attention to detail
Intermediate clinical study design
Intermediate clinical trials knowledge
Intermediate forecasting
Intermediate interpersonal skills
Intermediate oral and written communications
Intermediate process improvement
Intermediate project management
Intermediate regulatory compliance
Prior clinical research experience preferred

Benefits

Comp & perks

Total rewards package supporting health, life, career, and retirement
Seasonal flu vaccination requirement with exceptions for religious beliefs or medical reasons
Required occupational-health vaccinations provided at no cost
Accommodation support during the pre-employment process
Consideration for applicants completing their final academic semester/quarter
Pre-employment background-check process