Central Monitor

Piper Companies is seeking a Central Monitor (Remote) to support operations remotely. This role will focus on managing risk-based quality and centralized monitoring for clinical trials, ensuring compliance, data analysis, and cross-functional collaboration. Responsibilities for the Central Monitor (Remote) include: • Develop and manage risk-based quality and monitoring processes. • Lead risk assessment, define KRIs/QTLs, and review data for issues. • Train teams and collaborate on centralized monitoring best practices. • Ensure compliance and drive process improvements and audit readiness. Qualifications for the Central Monitor (Remote) include: • 3+ years central monitoring experience in a CRO setting; prior CRA on-site monitoring experience preferred. • Expert in ICH GCP and regulations, with focus on Risk-Based Quality Management and Central Monitoring updates. • Proficient in central monitoring technologies, processes, and clinical research databases/systems/tools. • Leadership and communication skills: experience mentoring teams, writing procedures, and advising on best practices; strong facilitation, problem-solving, and attention to detail. • Background in Infectious Disease clinical trials and/or Oncology; government contract experience is a plus. Compensation for the Central Monitor (Remote) include: • Salary Range: $85,000 - $115,000 based on years of experience • Benefits: Medical, Dental, Vision, 401k Plan, PTO (Paid Time Off), Holidays, Sick leave as required by law This job opens for applications on 12/11/2025. Applications for this job will be accepted for at least 30 days from the posting date Keywords: Risk-Based Quality Management, Centralized Monitoring, Clinical Trials, KRIs, QTLs, Risk Assessment, Protocol Review, Data Analysis, Dashboards, Signal Management, Action Management, Clinical Risk Management, Operational Risk Log, Subject Matter Expert, SME, FDA Regulations, ICH GCP, Regulatory Compliance, SOP Development, Quality Management System, Inspection Readiness, Audit Preparation, Process Improvement, Proposal Writing, Budget Development, Bid Defense, Cross-Functional Collaboration, CRA, Clinical Project Management, Clinical Trial Management, Data Management, Data Analytics, Clinical Research, Monitoring Technologies, Database Systems, Mentorship, Training, Facilitation Skills, Presentation Skills, Problem-Solving, Conflict Resolution, Attention to Detail, Infectious Disease, Oncology, Medical Device, Government Contracts, Therapeutics, Vaccines, Remote Work, Maryland, Virginia, Washington D.C., CRO Experience, Clinical Monitoring, Best Practices. Apply tot his job