Overview As a Principal, Study Start Up Associate at ICON, you lead clinical trial start-up and site activation efforts to ensure regulatory compliance and timely activation. You will work with cross-functional teams to streamline processes and build start-up capability, guiding sites and study teams through early-phase activities. You’ll stay ahead of regulatory trends to refine strategies and best practices, contributing to ICON’s mission of delivering medicines to patients faster. This role offers exposure to integral trials and a chance to shape start-up operations at scale.

Compensaciones / BeneficiosCompetitive base salaryPerformance-related incentivesHealth and wellbeing programmes (medical, dental, vision)Retirement and pension plansLife assurance and disability coverageEmployee assistance programmes and wellbeing resources ResponsabilidadesLead preparation and submission of essential regulatory documents for approvals and site activationCollaborate with cross-functional teams (PM, clinical operations, regulatory affairs)



to streamline start-up processesOversee site identification and activation to meet project criteria and compliance standardsProvide guidance and support to study teams and sites during start-up, fostering communication and collaborationStay updated on industry regulations and trends to enhance start-up strategies and best practices Requisitos principalesBachelor's degree in a relevant scientific discipline or healthcare-related fieldExtensive experience in study start-up activities within clinical researchProven ability to manage multiple projects and prioritize in a fast-paced environmentExcellent organizational skills and attention to detailStrong communication and interpersonal skills for diverse stakeholdersCommitment to high standards of quality and compliance in start-up activitiesWillingness to travel approximately 15%strong communicationteam leadershipcross-functional collaborationregulatory affairs knowledgeclinical trial start-up processessite identification and activation

📌 Clinical Trial Submission Coordinator (Barcelona)
🏢 Jobrapido
📍 Barcelona