Remote RBQM & Central Monitoring Manager

Worldwide Clinical Trials; Miami (FL); À distance; USD 66 000 - 131 000; Plein temps

Avantages offerts par ce poste

Transparent compensation

Competitive benefits

Résumé du poste

Worldwide Clinical Trials is seeking a Risk and Central Monitoring Associate Manager to drive RBQM, RBM and central monitoring across multiple studies. You will lead risk assessments, develop central monitoring plans, and ensure study teams implement quality controls in line with ICH GCP.

This remote role supports global teams with cross-functional collaboration, KRIs, QTLs, dashboards and training, delivering inspection-ready processes and transparent compensation.

Qualifications

• BSc, RN, or an equivalent combination of education, skills, and experience.
• At least 4 years of clinical research experience, including a minimum of 3 years of experience with Risk-Based Monitoring (RBM).
• Experience as a Central Monitor or within a Central Monitoring function is preferred.
• Strong understanding of RBQM principles, study risk assessments, centralized monitoring, KRIs, and QTLs.
• Excellent data analysis, trend identification, and problem-solving abilities.
• Experience collaborating across functions within global project teams.
• Strong communication, presentation, planning, and organizational skills.
• Proficiency in English and Microsoft Office and clinical technology systems.

Responsabilités

• Lead and oversee Risk-Based Quality Management (RBQM) activities for assigned clinical studies.
• Develop and maintain Central Monitoring Plans with 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 KRIs and QTLs.
• Perform centralized monitoring reviews to identify trends, outliers, signals, and risks and recommend actions.
• Maintain central monitoring dashboards and support monitoring activities throughout the study lifecycle.
• Deliver training and guidance on RBQM strategies, monitoring approaches, and risk management processes.
• Contribute to inspection readiness, budget awareness, sponsor interactions, audits, and related meetings.

Connaissances

RBQM principles

Central Monitoring

RBM experience

Data analysis

Cross-functional teamwork

English proficiency

MS Office

Formation

BSc

RN

Outils

Microsoft Office

Description du poste

Worldwide Clinical Trials is seeking a Risk and Central Monitoring Associate Manager to drive RBQM, RBM and central monitoring across multiple studies. You will lead risk assessments, develop central monitoring plans, and ensure study teams implement quality controls in line with ICH GCP.

This remote role supports global teams with cross-functional collaboration, KRIs, QTLs, dashboards and training, delivering inspection-ready processes and transparent compensation.