Overview 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 is advancing the development of medicines, biologic therapies, and vaccines for challenging diseases such as cancer, cardio-metabolic diseases, Alzheimer’s, and infectious diseases. Be prepared to work in a collaborative environment driven by innovation and continuous improvement. Responsibilities 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 training for CRAs, Investigators, and Study Coordinators. Monitoring vendor activities, including laboratories and equipment provisioning. Contributing to the Country Operational Plan (COP) and collaborating with DFM and GCMs to ensure local delivery of the study. Approving Baseline and Revised Enrolment 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 appropriately. Resolving cross-functional study issues. Escalating issues related to delivery, timelines, or budgets to GCMs or TMT as appropriate. Preparing for regulatory inspections, including TMF review and storyboard creation. Collaborating with local teams to ensure study delivery aligns with global expectations. Identifying and mitigating risks, and informing relevant teams proactively. Qualifications You are: Holding a bachelor’s degree in health, life sciences, or a related field. Having at least 5 years of experience in clinical research or a related field. Possessing financial knowledge relevant to clinical trials. Experienced in overseeing external vendors such as CROs, labs, and imaging providers. What ICON can offer you: Our success depends on our people. We prioritize building a diverse culture that rewards high performance and nurtures talent. Along with a competitive salary, ICON offers benefits focused on well-being and work-life balance. Visit our careers website to learn more: https://careers.iconplc.com/benefits ICON values inclusion and belonging, providing an accessible environment for all candidates. We are committed to non-discrimination and equal opportunity employment. If you require accommodations during the application process, please inform us through the provided form. Interested but unsure if you meet all requirements? We encourage you to apply — you might be exactly what we’re looking for at ICON, whether for this or other roles. #J-18808-Ljbffr