Central Monitor

Central Monitor

Job AttributesJob Id:

166301

Job Category:

Job Location:

bethesda,

MarylandSecurity Clearance:

No ClearanceBusiness Unit:

Piper CompaniesDivision:

Piper Clinical SolutionsPosition Owner:

MacKenzie UpdikePiper Companies is looking for a Central Monitor to join a clinical research organization (CRO) company located in Bethesda, MD.Responsibilities of the Central Monitor include:

• Develop and maintain risk-based quality management and centralized monitoring processes, templates, and tools for corporate and trial-specific use
• Review study protocols to confirm feasibility of KRIs and QTLs setup, reporting, and standardization requirements
• Lead risk assessments for studies and recommend protocol-specific risk indicators for centralized monitoring
• Assist with configuration and validation of centralized monitoring data analysis platforms
• Analyze clinical study data to identify potential site performance or organizational issues and provide recommendations for CRA follow-up
• Train project teams on interpreting central monitoring signals and making informed decisions for study conduct
• Maintain and update operational risk logs for clinical risk management activities
• Provide guidance, mentorship, and coordination for all centralized monitoring tasks
• Monitor dashboards and outputs, suggest actions for signal management, and ensure timely resolution with study teams
• Act as the SME for central monitoring during dashboard development and implementation
• Advise clients and sponsors on best practices for centralized monitoring in a client-facing capacity
• Collaborate effectively with CRAs, Clinical Project Managers, Trial Managers, and Data Management teams
• knowledge of regulatory requirements (FDA, ICH/GCP), data analysis, and statistical principles in central monitoring activities
• Support government and commercial contracts across multiple therapeutic areas, including infectious disease, oncology, and medical devices
• Report program status and potential risks to leadership and recommend mitigation strategies
• Ensure adnce to documented processes and timelines, and take corrective action to prevent delays
• Maintain accuracy and attention to detail in a fast-paced environment with shifting priorities
• Comply with Quality Management System policies and procedures
• Contribute to corporate initiatives such as SOP development, process improvement, proposal writing, and bid defense meetings
• Assist with audit preparation, inspection readiness, and post-inspection follow-up activities Qualifications for the Central Monitor include:
• Strong understanding of ICH GCP and regulatory requirements, with emphasis on Risk-Based Quality Management and Central Monitoring
• Minimum of 3 years of experience in centralized monitoring within a CRO environment
• Previous experience as a CRA performing on-site monitoring or equivalent skill set
• Familiarity with centralized monitoring database systems and processes
• Proven ability to lead or mentor teams, develop procedures, and advise on best practices and tools for central monitoring
• Excellent facilitation, presentation, and problem-solving skills; strong written and verbal communication; attention to detail and quality control; and experience with clinical research systems and tools
• Background in infectious disease or oncology trials, or prior work on government contracts, is preferred
• Bachelor's degree required

COVID-19

vaccination (first and second dose) required Compensation for Central Monitor includes:

Rate Range:

$85,000-$125,000, depending on experience

Comprehensive Benefit Package:

Cigna Medical/Dental/Vision, 401K, Sick Leave as Required by Law This job is open for applications on May 18th, 2026. Applications will be accepted at least 30 days from the posting date.

Keywords:

Central Monitoring, Risk-Based Quality Management, Clinical Trials, ICH GCP, KRIs, QTLs, Clinical Risk Management, CRO, CRA, Data Analysis, FDA Regulations, Oncology, Infectious Disease, Clinical Research, Remote, Bethesda MD #LI-MU1 #LI-ONSITE...Visit the Employer site for more details