Experteer Overview
Si le interesa solicitar este empleo, por favor, asegúrese de cumplir los siguientes requisitos que se enumeran a continuación.
As Site Activation Lead, you drive study start-up from plan to activation, safeguarding timelines, budgets, and patient access. You’ll coordinate regulatory submissions, site contracts, and risk mitigation while guiding regional teams to align with sponsor expectations. This role sits at the heart of accelerating trial activation and patient access, partnering with sponsors from day one and ensuring consistent, milestone-driven performance.
Compensaciones / Incentivos
• Design and lead Study Start-Up Plans with clear timelines and alignment across countries
• Drive regulatory and ethics submissions to approval to accelerate activation
• Oversee site contracts and budget negotiations to avoid delays
• Identify risks early and implement mitigation strategies
• Partner with sponsors at Bid Defences and Kick-Off Meetings to align strategy




• Lead and empower regional start-up teams for consistent performance
• Ensure data accuracy, reporting, and KPI tracking for transparency and control
• Influence time-to-activation and ultimately time-to-treatment for patients
Responsabilidades
• 5+ years in Clinical Research with strong Study Start-Up experience
• Deep understanding of regulatory frameworks and submission processes
• Proven ability to lead xqbhyrx cross-functional teams globally
• Strong project management and risk mitigation skills
• Confidence in sponsor-facing environments
Requisitos principales
• Competitive base salary
• Health and wellbeing programmes (medical, dental, vision)
• Retirement and pension plans
• Life assurance and disability coverage
• Employee assistance programmes and wellbeing resources
• Learning and development opportunities

📌 Site Activation Lead (Barcelona)
🏢 Icon Clinical
📍 Barcelona