Remote Risk & Central Monitoring Lead

Worldwide Clinical Trials; Saint Paul (MN); Remote; USD 66,000 - 131,000; Full time

Benefits offered by this job

Transparent compensation

Job summary

Worldwide Clinical Trials is seeking a Risk and Central Monitoring Associate Manager to lead RBQM activities across clinical studies, developing monitoring plans and guiding risk assessments. This remote role requires RBM experience and strong data analysis, with collaboration across global teams to maintain study quality and regulatory readiness.

Candidates will spearhead KRIs/QTLs, oversee centralized monitoring reviews, and contribute to training, dashboards, and sponsor communications.

Qualifications

• BSc, RN, or an equivalent combination of education, skills, and experience.
• 4+ years of clinical research experience with RBM, RBQM knowledge.
• Experience as Central Monitor or in Central Monitoring.
• Strong RBQM principles, risk assessments, centralized monitoring, KRIs, QTLs.
• Ability to analyze data, identify trends, and apply critical thinking.
• Collaborative work across global teams and strong communication.

Responsibilities

• Lead RBQM activities for assigned studies.
• Develop and maintain Central Monitoring Plans with approvals.
• Support study risk assessments with cross-functional teams.
• Track and monitor KRIs and QTLs.
• Perform centralized monitoring reviews and recommend actions.
• Maintain central monitoring dashboards and ongoing activities.
• Deliver RBQM training to study teams and ensure compliance.
• Support inspection readiness, audits, and sponsor interactions.

Skills

RBQM

Central Monitoring

RBM

Risk assessment

Data analysis

Cross-functional collaboration

Communication

MS Office

Education

BSc, RN, or equivalent

Tools

Clinical technology systems

Job description

Worldwide Clinical Trials is seeking a Risk and Central Monitoring Associate Manager to lead RBQM activities across clinical studies, developing monitoring plans and guiding risk assessments. This remote role requires RBM experience and strong data analysis, with collaboration across global teams to maintain study quality and regulatory readiness.

Candidates will spearhead KRIs/QTLs, oversee centralized monitoring reviews, and contribute to training, dashboards, and sponsor communications.