
Clinical Research Site Manager, Neurology
Posted 5 days ago

Posted 5 days ago
This is a fully remote position, open to applicants in Maryland.
• Oversee the execution of large-scale, multicenter clinical trials at the site level across a nationwide network of collaborating clinical sites.
• Lead the processes of site startup, feasibility assessments, resource readiness evaluations, activation timelines, and onboarding for centralized IRB/master agreements.
• Establish effective communication with clinical teams throughout the phases of identification, selection, preparation, and activation.
• Drive enrollment performance, monitor site-level metrics, identify underperforming sites, and create tailored remediation strategies.
• Manage relationships with investigators and sites; set expectations, assign deliverables, and ensure accountability.
• Direct and oversee daily activities related to eligibility, randomization, adherence to protocols, safety reporting, and compliance with investigational products.
• Ensure timely and accurate submissions to IRBs, sponsors, ethics committees, and master agreements.
• Conduct teleconferences, training sessions, and mentoring for coordinators and investigators.
• Provide support to quality assurance monitors.
• Manage site startup and performance plans, quality reviews, resource requirements, escalations, and deadlines.
• Implement lean management processes to deliver trials on schedule, within budget, and to high-quality standards.
• Perform self-audits and site audits; recommend improvements to operations and protocols.
• Track proposals and documentation through the signature and approval processes.
• Utilize statistical, quantitative, explanatory, and predictive analysis to inform decision-making.
• Assist investigators in interpreting performance-based data.
• Facilitate meetings among project stakeholders and leadership.
• Maintain professional project documentation and deliverables.
• Develop standard operating procedures (SOPs) and assist with study-site auditing and monitoring.
• Stay informed about evolving clinical research technologies and support the adoption of innovations.
• Act as a liaison between leadership and research communities.
• Perform other duties as assigned.
• Bachelor’s Degree in a related field.
• Five years of relevant experience in 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 or equivalent, as per the JHU equivalency formula.
• Prior experience in clinical research is preferred.
• Intermediate analytical skills.
• Intermediate attention to detail.
• Intermediate skills in clinical study design.
• Intermediate knowledge of clinical trials.
• Intermediate forecasting abilities.
• Intermediate interpersonal skills.
• Intermediate oral and written communication skills.
• Intermediate skills in process improvement.
• Intermediate project management skills.
• Intermediate knowledge of regulatory compliance.
• Successful candidates will be subject to a pre-employment background check.
• Faculty, staff, and students are required to receive the seasonal flu vaccine, subject to stated exceptions.
• Comprehensive rewards package supporting employees' health, life, career, and retirement needs.
• Seasonal flu vaccine provided, with exemptions for medical and religious reasons.
• Required occupational health vaccinations provided at no cost.
• Remote work arrangement available.
• Monday to Friday schedule, from 8:30 am to 5:00 pm.
• Pre-employment accommodation support offered.
• Commitment to equal opportunity employment.
Thermo Fisher Scientific
ICON plc
ICON plc
Clinical Outcomes Solutions
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