Risk and Central Monitoring Associate Manager

Added
less than a minute ago
Type
Full time
Salary
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Related skills

data analysis gcp clinical research risk assessment kri

πŸ“‹ Description

  • Lead and oversee Risk-Based Quality Management (RBQM) activities for assigned clinical studies
  • Develop, maintain, and coordinate approvals for Central Monitoring Plans that reflect
  • Support the development, assessment, and ongoing review of study risk assessments in collaboration
  • Facilitate the identification, tracking, evaluation, and monitoring of Key Risk Indicators (KRIs)
  • Conduct centralized monitoring reviews to identify trends, data outliers, emerging signals, and
  • Recommend appropriate follow-up actions and risk mitigation strategies based on monitoring findings

🎯 Requirements

  • Bachelor's degree in a relevant field, a registered nursing qualification (RN), or an equivalent
  • At least four years of experience in clinical research, including a minimum of three years working
  • 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
  • Knowledge of clinical trial quality oversight and the application of risk-based approaches
  • Demonstrated ability to analyze complex clinical data, identify trends and anomalies, assess

🎁 Benefits

  • Fully remote work arrangement for eligible candidates based in Brazil, with collaboration across
  • Full-time employment opportunity.
  • Competitive compensation based on relevant experience, education, performance, and internal equity.
  • A competitive benefits package, with specific offerings depending on the candidate's location.
  • Commitment to pay transparency, pay equity, and compliance with applicable employment laws.
  • Opportunity to contribute to clinical research initiatives focused on improving patient outcomes
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