Global CTA ICON 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. We are currently seeking a Global CTA to join our diverse and dynamic team. As a global CTA at ICON, you will assist with local project management activities of a clinical trials in a country or countries with operational aspects of assigned projects at the country level for end-to-end project management from start-up through to closeout activities What you will be doing Assist in the planning, execution, and monitoring of clinical trials, ensuring adherence to protocol requirements, regulatory guidelines, and industry standards. Schedules study management team meetings for each project assigned and maintains documentation from meetings in appropriate repository. Assists in management of project budgets and Affiliate spend, reconciliation of invoices, final budget and liaises with Accounts payable, as necessary. Coordinate study activities including site initiation, patient recruitment, data collection, and monitoring visits to ensure timely and accurate data collection and documentation. Collaborate with cross-functional teams including Clinical Operations, Data Management, and Biometrics to support the successful execution of clinical trials. Maintain comprehensive study documentation and records, ensuring compliance with applicable regulations and standard operating procedures. Support study close-out activities including data cleaning, analysis, and preparation of clinical study reports. Your profile Bachelor's or advanced degree in Life Sciences, Health Sciences, or a related field. Previous experience in clinical research or healthcare, within the pharmaceutical, biotechnology, or CRO industry. Experience in a similar role working in across multiple countries Strong organizational and time management skills, with the ability to prioritize tasks and manage competing priorities effectively. Excellent attention to detail and problem-solving abilities, with a commitment to ensuring data accuracy, integrity, and compliance. Effective communication and interpersonal skills, with the ability to collaborate cross-functionally and build strong relationships with study teams and clinical sites. Employment with ICON is contingent upon having the legal right to work in the country where the role is based. Rewards & Benefits ICON 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 location. Visit our careers site to read more about the benefits ICON offers. Inclusion and Accessibility ICON 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