Risk and Central Monitoring Associate Manager

Worldwide Clinical Trials

. Lead and oversee Risk-Based Quality Management (RBQM) activities for assigned clinical studies .

Posted 10/12/2026full-timeRemote • United States, Brazil, Canada, MexicoMid-Level💰 $65,500 - $130,500 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in Risk-Based Quality Management (RBQM) and centralized monitoring, with a strong ability to analyze data, identify trends, and implement risk management strategies in clinical studies. Proficient in collaborating with cross-functional teams and maintaining inspection readiness throughout the study lifecycle.

Highest-signal resume keywords

Risk-Based Quality Management (RBQM)Central Monitoring PlansKey Risk Indicators (KRIs)Risk-Based Monitoring (RBM)Clinical Research Experience

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical ResearchData AnalysisRisk AssessmentCentralized MonitoringTrend Identification

Soft Skills

CommunicationPresentationPlanningOrganizational SkillsCritical Thinking

Tools & Technologies

Microsoft OfficeClinical Technology Systems

Industry Keywords

ICH GuidanceQuality Tolerance Limits (QTLs)Inspection ReadinessGlobal Project TeamsSponsor Interactions

About the role

Key responsibilities & impact

Lead and oversee Risk-Based Quality Management (RBQM) activities for assigned clinical studies
Develop and maintain Central Monitoring Plans, ensuring appropriate approvals and alignment with study strategies
Support creation and ongoing review of study risk assessments with cross-functional teams
Facilitate identification, tracking, and monitoring of Key Risk Indicators (KRIs) and Quality Tolerance Limits (QTLs)
Perform centralized monitoring reviews to identify trends, outliers, signals, and potential risks, recommending actions to study teams
Maintain central monitoring dashboards and support ongoing monitoring throughout the study lifecycle
Deliver training and guidance to study teams on RBQM strategies, monitoring approaches, and risk management processes
Contribute to inspection readiness, budget awareness, sponsor interactions, audits, and project-related meetings
Collaborate with global teams and internal stakeholders and sponsors to support inspection-ready processes and clinical trial quality

Requirements

What you’ll need

BSc, RN, or an equivalent combination of education, skills, and experience
At least 4 years of clinical research experience
Minimum of 3 years of experience with Risk-Based Monitoring (RBM) and associated ICH/regulatory guidance
Prior experience working as a Central Monitor or within a Central Monitoring function
Strong understanding of RBQM principles, study risk assessments, centralized monitoring, KRIs, and QTLs
Ability to analyze complex data, identify trends and risks, and apply critical thinking to problem-solving and issue resolution
Experience collaborating across functions and working effectively within global project teams
Strong communication, presentation, planning, and organizational skills
Proficiency in English
Strong proficiency with Microsoft Office and clinical technology systems

Benefits

Comp & perks

Competitive benefits package depending on location
Inclusive and equitable workplace
Transparent compensation and pay equity