Global Study Associate Director – CVRM

• Lead global study teams to deliver cardiovascular clinical trials across the study lifecycle
• Drive study timelines, budgets, quality objectives, and key milestones
• Serve as the primary operational contact for study teams, CROs, and external partners
• Oversee outsourced activities, ensuring effective vendor management and study oversight
• Lead study planning, risk management, issue resolution, and escalation activities
• Ensure TMF quality and inspection readiness
• Manage study budgets, forecasting, and operational reporting
• Support audits, regulatory inspections, and process improvement initiatives
• Lead delivery of global cardiovascular and cardiometabolic clinical trials

• Degree in Life Sciences, Clinical Research, or a related field
• Significant global experience within pharmaceutical or biotechnology clinical development
• Proven experience leading global clinical studies and cross-functional teams
• Strong knowledge of ICH-GCP, clinical trial regulations, and study management principles
• Experience managing study budgets, vendors, timelines, and operational risks
• Excellent leadership, stakeholder management, communication, and organisational skills
• Experience supporting cardiovascular or cardiometabolic clinical trials is highly desirable
• Advanced degree (Master's, PhD, or equivalent) preferred
• Project Management certification preferred
• Experience delivering large-scale global studies across multiple phases of development preferred
• Previous involvement in cardiovascular outcomes studies or late-phase cardiovascular trials advantageous
• Legal right to work in France

• Competitive base salary and performance related incentives
• Health and wellbeing programmes including medical, dental, and vision coverage where applicable
• Retirement and pension plans
• Life assurance and disability coverage
• Employee assistance programmes and wellbeing resources
• Learning and development opportunities through structured training and career pathways