Risk and Central Monitoring Associate Manager

Join a global clinical research environment dedicated to advancing medical innovation and improving patient outcomes. In this role, you will help strengthen clinical trial quality by leading risk-based quality management (RBQM) activities and supporting centralized monitoring strategies across assigned studies. You will collaborate with multidisciplinary teams and sponsors to identify potential risks, evaluate clinical data, and develop proactive mitigation approaches. Through the use of key risk indicators, quality tolerance limits, and monitoring dashboards, you will help teams make informed, data-driven decisions throughout the clinical trial lifecycle. You will also contribute to regulatory compliance, inspection readiness, and consistent quality standards aligned with ICH Good Clinical Practice guidelines. This remote opportunity offers the chance to work with international teams and make a meaningful contribution to reliable, high-quality clinical research.

• Bachelor's degree in a relevant field, a registered nursing qualification (RN), or an equivalent combination of education, skills, and professional experience.

• At least four years of experience in clinical research, including a minimum of three years working with Risk-Based Monitoring (RBM) and associated ICH guidelines or regulatory guidance.

• Previous experience working as a Central Monitor or within a Central Monitoring function.

• Strong understanding of Risk-Based Quality Management (RBQM), study risk assessments, centralized monitoring processes, KRIs, and QTLs.

• Knowledge of clinical trial quality oversight and the application of risk-based approaches throughout the study lifecycle.

• Demonstrated ability to analyze complex clinical data, identify trends and anomalies, assess potential risks, and recommend appropriate actions.

• Strong critical-thinking and problem-solving skills, with the ability to investigate issues and support effective resolution.

• Experience collaborating across functional teams and contributing to global clinical research projects.

• Excellent communication and presentation skills, with the ability to explain monitoring findings and risk management strategies to diverse stakeholders.

• Strong planning, organizational, and time management skills, including the ability to coordinate multiple activities and priorities.

• Proficiency in English, with the ability to communicate effectively in an international working environment.

• Strong proficiency in Microsoft Office applications and familiarity with clinical research technology systems.

• Ability to work independently in a remote setting while maintaining effective collaboration across multiple teams and time zones.