Senior CM Analyst II

• Identify and characterize issues and trends in operational and patient clinical trial data using analytical or statistical tools
• Leverage operational experience and knowledge to evaluate issues and develop findings based on analyzed data
• Communicate issues and potential risks to project team members for follow-up action
• Conduct risk assessments and develop monitoring plans
• Support sponsor oversight, trend analysis, signal detection, and site monitoring strategy
• Ensure regulatory compliance and inspection readiness
• Work within a Functional Service Partnership dedicated to a specific pharmaceutical client

• Degree in Life Sciences or a related field, or equivalent professional experience as permitted by the approved job description
• 3 years of experience, as indicated in the client's job description, subject to confirmation against the requirements for the Sr CM Analyst II level
• Strong knowledge of Site Monitoring and Site Management
• Strong communication skills
• Leadership capabilities
• Experience working with cross-functional teams
• Knowledge of risk assessments, monitoring plans, sponsor oversight, trend analysis, signal detection, site monitoring strategy, regulatory compliance, and inspection readiness

• Collaboration and development opportunities
• Opportunity to contribute to scientific excellence and organizational performance
• Membership in a global team
• Opportunity to work with pharmaceutical and biotechnology clients on clinical trials