Clinical Research Site Manager, Neurology
Employment Information
Report this job
Job expired or something wrong with this job?
Job Description
Clinical Research Site Manager overseeing startup, enrollment, compliance, and performance across neurology clinical-trial sites for Johns Hopkins University. Remote role based in the Baltimore, Maryland area.
Responsibilities:
- 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:
- 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:
- 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
Similar Jobs
Clinical Research Development Analyst
Clinical Research Development Analyst supporting clinical trial strategies, protocols, and regulatory dossiers. Contributing to new medicine approvals and clinical data generation at Libbs Farmacêutica.
Early Clinical Scientist – Translational Medicine
Early Clinical Scientist coordinating early-phase clinical trials for Parexel’s clinical development services. Overseeing safety, data validity, CRO performance, and trial documentation.
Clinical Trial Manager, Class III Medical Devices
Clinical Trial Manager coordinating Class III implantable-device trials at Biogen, a biotechnology company. Managing sites, vendors, compliance, risks, and regulatory workflows.
Clinical Research Lead
Clinical Research Lead managing investigators, sites, enrollment, and vendor oversight for ICON’s sponsor-dedicated clinical research programs in the UK.
Clinical Research Associate II
Clinical Research Associate II monitoring oncology clinical trials for PSI, a contract research organization. Managing site visits, data integrity, regulatory documents, and investigator communications.
Biostatistician, Neurology
Biostatistician analyzing longitudinal neurology data for Johns Hopkins School of Medicine. Developing SAS/R analyses, datasets, statistical plans, and publication-ready results.
Senior Clinical Research Associate
Senior Clinical Research Associate monitoring clinical trials for Precision for Medicine, a specialized clinical research organization. Coordinating study setup, site visits, regulatory compliance, client support, and junior staff mentoring.
Senior Clinical Research Associate
Senior Clinical Research Associate monitoring clinical trials for Precision for Medicine, a specialized CRO. Ensuring protocol compliance, site oversight, and sponsor collaboration across Spain.
Senior Clinical Research Associate
Senior Clinical Research Associate monitoring clinical trials for Precision for Medicine, a specialized CRO. Coordinating study setup, site monitoring, regulatory activities, clients, and junior CRA mentoring.
Clinical Research Associate II
Clinical Research Associate II advancing AbbVie’s oncology clinical trials. Monitoring investigative sites, protecting patient safety, and improving data integrity for innovative medicines.
Clinical Trial Manager, Regulatory Experience
Clinical Trial Manager overseeing site monitoring, regulatory compliance, and clinical data quality for Syneos Health’s biopharmaceutical research services. Supporting trial delivery, audits, recruitment, and site teams.
Clinical Trial Manager
Clinical Trial Manager overseeing study start-up, CRAs, vendors, budgets, and clinical deliverables. Supporting Linical’s CRO mission to provide clinical-trial expertise.
Senior Clinical Research Associate
Senior Clinical Research Associate at AbbVie, a biopharmaceutical company developing innovative medicines and health solutions. Overseeing clinical study sites, monitoring, regulatory compliance, audits, and CRA mentoring in Taiwan.
Clinical Research Associate II – Immunology
Clinical Research Associate monitoring immunology clinical trials for AbbVie, an innovative medicines company. Ensuring site compliance, data integrity, patient safety, and recruitment performance.
Senior Clinical Research Associate
Senior Clinical Research Associate monitoring vaccine trials for ICON, a global clinical research organisation. Overseeing sites, compliance, data integrity, and trial execution in Buenos Aires remotely.
Clinical Research Site Manager, Neurology
Clinical research site manager coordinating startup, enrollment, compliance, and performance across neurology trials for Johns Hopkins University. Remote role managing external clinical sites and investigators.
Clinical Research Associate II, Bilingual
Clinical Research Associate monitoring pharmaceutical trials for protocol compliance and data integrity. Conducting remote and on-site site visits across Canadian investigational sites.
Senior Biostatistician
Senior Biostatistician supporting ophthalmic clinical trial design, analysis, and reporting at Lexitas. Ensuring statistical integrity across clinical studies, submissions, and publications.
Clinical Research Feasibility Coordinator
Clinical research coordinator assessing trial feasibility, investigators, site capabilities, and budgets for Alcanza’s multi-site clinical research network. Supporting Business Development across Phase I-IV studies.
Clinical Research Associate II – Sponsor-dedicated
Clinical Research Associate monitoring clinical trial sites for Syneos Health, a fully integrated life sciences services organization. Ensuring GCP compliance, data integrity, and study delivery.