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.

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 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 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 field

Extensive 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 effectively in a fast-paced environment.

Excellent organizational skills and attention to detail, with a commitment to delivering high-quality results.

Strong communication and interpersonal skills, enabling effective collaboration with diverse teams and external stakeholders.A commitment to maintaining high standards of quality and compliance in all study start-up activities.

Willingness to travel as required (approximately 15%)Employment with ICON is contingent upon having the legal right to work in the country where the role is based.

Rewards & BenefitsICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.

Benefits may include: Competitive base salary and performance related incentives

Health and wellbeing programmes including medical, dental, and vision coverage where applicable

Retirement and pension plans

Life assurance and disability coverage

Employee assistance programmes and wellbeing resources

Learning and development opportunities through structured training and career pathways

Benefits may vary depending on role and our careers site to read more about the benefits ICON offers.

Inclusion and AccessibilityICON is an equal opportunity employer.

We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.

If you require reasonable accommodations during the recruitment process, please let us know or submit a request here.

Are you a current ICON Employee? Please click here to apply

Summary

Location: Spain, Madrid; Czech Republic, Prague; Hungary, Budapest; Spain, Barcelona

Type: Full time

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