Descripción del trabajo

Experteer 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 / Beneficios

Lead preparation and submission of essential regulatory documents for approvals and site activation
Collaborate with cross-functional teams (PM, clinical operations, regulatory affairs) to streamline start-up processes
Oversee site identification and activation to meet project criteria and compliance standards
Provide guidance and support to study teams and sites during start-up, fostering communication and collaboration




Stay updated on industry regulations and trends to enhance start-up strategies and best practices
Responsabilidades

Bachelor's degree in a relevant scientific discipline or healthcare-related field
Extensive experience in study start-up activities within clinical research
Proven ability to manage multiple projects and prioritize in a fast-paced environment
Excellent organizational skills and attention to detail
Strong communication and interpersonal skills for diverse stakeholders
Commitment to high standards of quality and compliance in start-up activities
Willingness to travel approximately 15%
Requisitos principales

Competitive base salary
Performance related incentives
Health and wellbeing programmes (medical, dental, vision)
Retirement and pension plans
Life assurance and disability coverage
Employee assistance programmes and wellbeing resources

📌 Clinical Trial Submission Coordinator (Madrid)
🏢 Icon Clinical
📍 Madrid