Team Manager – EMEA Clinical Trial Start-Up Lead

• Lead and oversee clinical trial start-up activities across multiple EU countries
• Coordinate country teams and cross-functional stakeholders in a matrix environment
• Provide regional oversight of site activation activities against timelines, quality expectations, and contractual commitments
• Navigate EU-CTR and country-specific regulatory and start-up requirements
• Manage country-specific documentation and additional national or local committee approvals
• Coordinate information flow among project teams, clients, country teams, functional departments, and site activation stakeholders
• Develop and implement start-up plans and guidelines using PPD/Thermo Fisher Scientific tools and processes
• Monitor and analyse project and country-level start-up status, metrics, escalations, and recommendations
• Identify and mitigate operational, regulatory, contractual, and timeline risks
• Manage competing priorities, dependencies, timelines, and critical-path activities across multiple countries
• Coordinate feasibility, site contracts, country teams, and related activities
• Manage financial and contractual aspects relating to site activation
• Control project resources and expenses against agreed budgets
• Evaluate complex start-up issues and implement agreed solutions
• Build effective relationships with customers and internal stakeholders throughout project delivery

• Bachelor’s degree or equivalent relevant academic/vocational qualification
• Typically 5+ years of relevant clinical research experience, or an equivalent combination of education, training, and directly related experience
• Demonstrated experience in clinical trial study start-up/site activation
• Demonstrated regional EU start-up leadership with direct operational responsibility across multiple EU countries
• Direct SSU/Study Start-Up leadership and oversight across multiple EU countries
• Practical knowledge of EU-CTR and its application to multi-country clinical trial start-up
• Understanding of country-specific EU-CTR implementation and documentation requirements
• Knowledge of additional national, local, institutional, or committee approvals outside the EU-CTR process
• Experience managing start-up risks and issues
• Ability to manage competing priorities across multiple countries
• Ability to lead, influence, liaise with, and coordinate cross-functional and geographically dispersed project teams
• Strong cross-cultural awareness
• Strong organisational, project management, and multitasking capabilities with excellent attention to detail
• Ability to identify contractual and operational risks and develop solutions
• Comprehensive understanding of clinical research and clinical development, including applicable guidelines, directives, study phases, therapeutic areas, and medical terminology
• Ability to work effectively in a fast-paced environment, manage changing priorities, communicate with diverse stakeholder groups, and perform under pressure
• Occasional travel availability, including outside normal business hours or at weekends

• Fully remote work arrangement
• Occasional domestic and international travel of up to approximately 20%
• Collaborative environment
• Opportunity to contribute to successful clinical studies and scientific breakthroughs