Overview 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 / BeneficiosCompetitive base salaryHealth and wellbeing programmes (medical, dental, vision)Retirement and pension plansLife assurance and disability coverageEmployee assistance programmes and wellbeing resourcesLearning and development opportunities ResponsabilidadesDesign and lead Study Start-Up Plans with clear timelines and alignment across countriesDrive regulatory and ethics submissions to approval to accelerate activationOversee site contracts and budget negotiations to avoid delaysIdentify risks early and implement mitigation strategiesPartner with sponsors at Bid Defences and Kick-Off Meetings to align strategyLead and empower regional start-up teams for consistent performanceEnsure data accuracy, reporting, and KPI tracking for transparency and controlInfluence time-to-activation and ultimately time-to-treatment for patients Requisitos principales5+ years in Clinical Research with strong Study Start-Up experienceDeep understanding of regulatory frameworks and submission processesProven ability to lead cross-functional teams globallyStrong project management and risk mitigation skillsConfidence in sponsor-facing environmentsCross-functional collaborationAccountability and leadershipProblem-solving and proactive decision-makingRegulatory submissions and ethics approvalsStudy Start-Up processesContract and budget negotiation

📌 Site Activation Lead (Barcelona)
🏢 Jobrapido
📍 Barcelona