Remote Risk-Based Monitoring Associate Manager

Worldwide Clinical Trials; Atlanta (GA); Remoto; USD 66.000 - 131.000; Tempo pieno

Descrizione del lavoro

Worldwide Clinical Trials is seeking a Risk and Central Monitoring Associate Manager for a REMOTE role. You will drive RBQM strategies, manage risk assessments, and oversee centralized monitoring across multi-time-zone teams to ensure study quality and compliance with ICH GCP guidelines.

Qualifications include a BSc or RN and 4+ years in clinical research with RBM experience, plus strong data analysis and cross-functional collaboration.

Competenze

• BSc, RN, or equivalent education/skills and experience.
• At least 4 years in clinical research with RBM and regulatory guidance.
• Experience as Central Monitor or in a Central Monitoring function.
• Strong RBQM principles, risk assessments, and KRIs/QTLs.
• Ability to analyze data, identify trends and risks.
• Experience collaborating across global project teams.
• Excellent communication, planning and organizational skills.
• Proficiency in English and Microsoft Office.

Mansioni

• Lead RBQM activities for assigned clinical studies.
• Develop and maintain Central Monitoring Plans with approvals.
• Support creation/review of study risk assessments with cross-functional teams.
• Monitor KRIs and QTLs.
• Perform centralized monitoring reviews and recommend actions.
• Maintain central monitoring dashboards.
• Deliver RBQM training to study teams.
• Support inspection readiness, budgets, audits and sponsor meetings.

Conoscenze

RBQM knowledge

Risk assessments

Centralized monitoring

KRIs and QTLs

Data analysis

Cross-functional collaboration

English communication

Formazione

BSc, RN

Strumenti

MS Office

Clinical technology systems

Descrizione del lavoro

Worldwide Clinical Trials is seeking a Risk and Central Monitoring Associate Manager for a REMOTE role. You will drive RBQM strategies, manage risk assessments, and oversee centralized monitoring across multi-time-zone teams to ensure study quality and compliance with ICH GCP guidelines.

Qualifications include a BSc or RN and 4+ years in clinical research with RBM experience, plus strong data analysis and cross-functional collaboration.