Risk Based Study Management Lead
Posted Oct 7
Posted Oct 7
This is a fully remote position, open to applicants in United Kingdom.
• Deliver comprehensive risk oversight for designated clinical studies.
• Lead and uphold study-specific risk assessments for assigned sponsor studies.
• Facilitate and preside over cross-functional risk review meetings.
• Foster proactive identification, discussion, and documentation of study-related risks.
• Collaborate with the Clinical Research Manager and study team on oversight and mitigation strategies.
• Analyze centralized monitoring outputs, Key Risk Indicators (KRIs), Key Performance Indicators (KPIs), and trends to identify emerging or systemic risks.
• Assist in issue escalation, root cause analysis, and risk mitigation planning.
• Ensure risk-based activities are in alignment with established principles and sponsor expectations.
• Support inspection readiness through clear documentation and defensible oversight decisions.
• Background in clinical trial operations, study management, monitoring, or centralized oversight.
• Strong grasp of risk-based monitoring and study management principles.
• Familiarity with ICH-GCP, regulatory standards, and quality frameworks.
• Exceptional facilitation skills with the confidence to lead cross-functional discussions.
• Analytical mindset with the capability to interpret data, trends, and signals.
• Outstanding communication and stakeholder management abilities.
• Capacity to work independently while effectively collaborating with sponsors and the ICON team.
• Legal authorization to work in the country where the position is located.
• Competitive base salary along with performance-related incentives.
• Comprehensive health and wellbeing programs, including medical, dental, and vision coverage where applicable.
• Retirement and pension plans.
• Life assurance and disability coverage.
• Employee assistance programs and wellbeing resources.
• Opportunities for learning and development through structured training and career pathways.
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