Study Start Up Manager - UKICON is a global 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 Manager, Study Start Up at ICON, you will lead and oversee the start-up activities for clinical trials, ensuring that all processes are completed efficiently and in compliance with regulatory requirements.What You Will Do:You will manage day-to-day site start-up and activation activities, supporting your team to deliver quality outcomes.Key responsibilities include:Managing and overseeing the end-to-end study start-up process, including site identification, feasibility, regulatory submissions, and site activation.Leading a team of study start-up professionals, providing guidance, mentorship, and support to ensure high performance and successful project delivery.Collaborating with sponsors, clinical operations, and regulatory teams to ensure compliance with local and global regulations and timelines for clinical trial initiation.Monitoring study start-up metrics, timelines, and budgets to ensure projects are delivered on time and within scope.Identifying potential risks and challenges in the start-up process and implementing strategies to mitigate delays or issues.Driving continuous improvement initiatives to optimize the study start-up process and enhance overall efficiency.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 clinical trial study start-up, with a strong understanding of global regulatory requirements and clinical operations.Proven leadership skills, with experience managing and mentoring teams in a fast-paced, deadline-driven environment.Excellent organizational and project management skills, with the ability to handle multiple studies and priorities simultaneously.Strong communication and stakeholder management skills, with the ability to collaborate effectively with sponsors and internal teams.Experience with process optimization and implementing best practices in study start-up activities.Willingness to travel as required (approximately 25%)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 incentivesHealth and wellbeing programmes including medical, dental, and vision coverage where applicableRetirement and pension plansLife assurance and disability coverageEmployee assistance programmes and wellbeing resourcesLearning and development opportunities through structured training and career pathwaysBenefits may vary depending on role and location.Visit 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 applySummaryLocation: UK, Reading; UK, SwanseaType: Full time
Manager, Study Start up in Swansea employer: Icon Clinical PLC
At ICON, we pride ourselves on being a values-driven organisation that fosters a collaborative and inclusive work culture. As an Operation Program Specialist, you will not only contribute to meaningful healthcare projects but also benefit from our comprehensive rewards package, including competitive salaries, health programmes, and robust career development opportunities. Join us in Sofia, Warsaw, or Swansea, where your expertise will be valued and your professional growth supported in a dynamic environment dedicated to bringing new treatments to patients faster.