As a Clinical Trial Manager, you will join the world’s largest & most comprehensive clinical research organization, powered by healthcare intelligence. You will partner with a global pharmaceutical client that advances the development of medicines, biologics, and vaccines for challenging diseases such as cancer, cardiovascular, Alzheimer’s, and infectious diseases. Be prepared to work in a partnership-driven environment focused on innovation and continuous improvement. What you will be doing: Planning, managing, and overseeing clinical study execution according to the global program strategy, leading the cross-functional Local Study Team (LST). Developing program/study-specific materials, such as monitoring plans and training documents. Setting site-level goals and managing study-specific deliverables for clinical sites within your country or countries. Leading or contributing to training for CRAs, Investigators, and Study Coordinators. Overseeing vendor activities, including laboratories and equipment provisioning. Providing country-level input into the Country Operational Plan (COP) and collaborating with the DFM and GCMs to ensure local study delivery. Approving baseline and revised enrollment plans at the country level. Monitoring study progress against timelines, deliverables, and budgets. Translating global startup requirements into local country targets. Reviewing data flow metrics, identifying trends, and following up as needed. Resolving cross-functional study-specific issues. Escalating issues related to delivery, timelines, or budgets to GCMs or TMT as appropriate. Preparing for regulatory inspections, including TMF reviews and storyboard generation. Collaborating with local teams to ensure alignment with global expectations. Identifying and mitigating risks, resolving issues at the country/site level, and informing relevant teams proactively and solution-oriented. You are: Holding a bachelor’s degree in health, life sciences, or a relevant field. Having at least 5 years of experience in clinical research or related areas. Possessing financial knowledge. Experienced in overseeing external vendors such as CROs, labs, and imaging vendors. What ICON can offer you: Our success depends on our people. We prioritize building a diverse culture that rewards high performance and nurtures talent. In addition to a competitive salary, ICON offers various benefits focused on well-being and work-life balance for you and your family. Learn more about working at ICON: https://careers.iconplc.com/benefits At ICON, inclusion and belonging are core to our culture. We are committed to providing an inclusive, accessible environment and a workplace free of discrimination and harassment. All qualified applicants will be considered equitably. If you need reasonable accommodations during the application process or to perform your duties, please let us know via this form . Interested but unsure if you meet all requirements? We encourage you to apply—your skills may be a perfect fit for this or other roles at ICON. #J-18808-Ljbffr