POL-Start Up- HBICON is a general 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 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 effectively in a fast-paced environment.Excellent organizational skills and attention to detail, with a commitment to delivering high-quality results.Strong communication and i