POL-Start Up- HBICON is a integral healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.

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As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.
As a Principal, Study Start Up Associate at ICON, you will be responsible for leading the start-up activities for clinical trials, ensuring efficient site activation and compliance with regulatory requirements.
What You Will Do:
Your focus will be on coordinating site start-up and activation delivery, resolving issues, and developing team capability.
Key responsibilities include:
Leading the preparation and submission of essential documents for regulatory approvals and site activation.
Collaborating with cross-functional teams, including project management, clinical operations,



and regulatory affairs, to streamline study start-up processes.
Overseeing the identification and selection of clinical sites, ensuring they meet project criteria and compliance standards.
Providing guidance and support to study teams and sites during the start-up phase, fostering effective communication and collaboration.
Staying current with industry regulations and trends to enhance start-up strategies and best practices.
Your Profile:
You will have solid site start-up and activation experience, with the ability to manage competing priorities and develop your team.
Required qualifications and experience: Bachelor's degree in a relevant scientific discipline or healthcare-related fieldExtensive experience in study start-up activities within the clinical research industry, with a strong understanding of regulatory requirements.
Proven ability to manage multiple projects and prioritize tasks effectiv

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