Global Study Manager - Oncology and/or Multi TA 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. Global Study Managers (GSMs) provide operational leadership across the full clinical study lifecycle, with accountability for the oversight and delivery of study management, site management, and vendor activities. In this role, you will lead global clinical trials from sourcing strategy and RFP development through study start-up, execution, database release, and inspection readiness—ensuring the timely delivery of high-quality data. As a key member of the core study team, you will represent the operational function, drive recruitment strategies and milestone delivery, and partner cross-functionally to align operational plans with overall study objectives. GSMs are responsible for leading and coordinating internal teams, external partners, and vendors to ensure successful study execution. This includes overseeing study-level plans, monitoring performance metrics, managing vendor scope and budgets, and proactively identifying and mitigating risks. You will play a critical role in driving decision-making, resolving site and operational challenges, and maintaining quality across all deliverables. The role requires strong leadership, the ability to work independently, and a collaborative approach, with opportunities to mentor team members and contribute to continuous improvement across study operations. What You Will Do: You will manage day-to-day project and program management activities, supporting your team to deliver quality outcomes. Key responsibilities include: Responsible to form, oversee and lead the operational sub team and request resources as needed Accountable for the development of realistic detailed study startup and/or study management strategy and monitoring plans, including Sourcing Strategy, input into Requests for Proposals, and for the selection of vendors Accountable for ensuring country-level feasibility is completed in collaboration with cross functional GSSO colleagues and Operational Analytics & Quantitative Sciences (OAQS) organization and pCRO (as applicable) reviewing Pre-trial Assessment outputs, approving sites, and assessing site activation plans Accountable and responsible to ensure PTMF setup for Study management and Country/Site level documents Inputs into the IQMP risk planning process for the study Coordinates development of study/protocol training & global investigator meetings. Accountable to ensure local Investigator meetings are coordinated by the Study Operational Manager (if assigned to study) and as applicable Develops and provides key inputs to Clinical Trial Budget (e.g., Per Subject Costs) Accountable to ensure Study Operational Managers are inputting into the budget for local/country level tasks (if assigned). The Global Study Manager will ensure cost variance, invoices, POs, etc. are reviewed in a timely manner ensuring spend is appropriate and on track with the forecast. Responsible for monitoring the budget and contracts for assigned vendors (e.g., central labs, ePRO, radiology, pCRO, etc.). Accountable for the delivery of the study against approved plans Leads inspection readiness activities related to study management and site readiness Support development and delivery of decentralized capabilities at investigator sites The Global Study Manager if assigned to study post database lock will ensure timely study closure and release of internal and external resources as appropriate. Development, review or approval of the Study Startup, Study Monitoring & protocol recruitment plans and others (e.g., CRF Guidelines, IMPALA manual, Training Plan, etc.) The Global Study Manager can delegate development of plans or components of plans to Study Operational Managers (if assigned) or CSTAs as appropriate. Approves & oversees drug supply management – manages flow of drug supply to the sites & set up Interactive Randomization Systems with Supply Chain Lead Accountable to ensure overall vendor oversight for vendors managed by Study Operational Managers (if assigned), action escalations related to vendor issues and escalate further as necessary Reviews consolidated Pre-trial Assessment reports, feasibility outputs, etc. in partnership with appropriate cross functional colleagues May support study level submission readiness May participate in vendor UAT and system set-up requirements review and approval (e.g., IRT, Central Lab) Responsible to ensure applicable system closure at study completion Leads and oversees all elements of study startup and monitoring functions to ensure delivery & compliance with all applicable Standard Operating Procedures (SOPs) and Quality Standards, interfacing directly with CRO Feasibility / Study Startup, Monitoring / Management & Site Contracting Groups Works proactively with data management functions and GSSO colleagues to ensure alignment on data flow and timely delivery. Regular review of data reports and dashboards to identify risks and drive appropriate actions. Shares and escalates plan deviations to Clinical Study Team Lead (and study team) and drives/oversees mitigations Review vendor expenses and WO as per study budget for assigned vendors (e.g., central labs, ePRO, radiology, pCRO etc.). Provides ongoing assessment of subject enrollment/discontinuations to inform accurate forecasting for financial planning Provides operational input into protocol design Leads Protocol Deviation trend review partnering with Clinical May lead and facilitates the routine study management vendor calls The Global Study Manager will be the technical expert for study management systems and processes The Global Study Manager will champion the implementation and use of harmonized, consistent processes, and excellence in Study Management deliverables related to cost-effective, timely, and high-quality clinical trial data according to agreed global goals. The Global Study Manager will be responsible for the technical oversight of the operational sub team to include but is not limited to standards, continuous improvement, issue escalation/resolution, inspection readiness/quality assurance, performance feedback, review of metrics. The Global Study Manager partners with the operational sub team and pCRO to proactively identify and resolve study operations staff performance issues. For project-specific audits and inspections, the Global Study Manager can serve as a resource to the study team in addition to the Study Operational Manager(s), if assigned, to facilitate the audit/inspection. Your Profile: Required qualifications and experience: Working knowledge of Good Clinical Practices, monitoring, clinical and regulatory operations A scientific or technical degree is preferred along with extensive knowledge of clinical trial methodology BA/BS 7+ years of relevant experience MBA/MS/ 6+ years of relevant experience Demonstrated clinical research experience and/or study management experience Demonstrated study management/leadership experience Demonstrated oversight of CROs/vendors Demonstrated experience in managing per subject costs, vendor & ancillary, and monitoring costs projections & spend Requires exceptional knowledge of own discipline and advanced knowledge of others and applies these skills to ensure a Sub Business Unit/Sub Operating Unit meets its goals Creates an environment where innovation is standard taking appropriate risks to advance innovative processes Develops ideas and leads complex projects across Sub Business Unit/Sub Operating Unit Develops innovative solutions to complex problems impacting a Sub Business Unit/Sub Operating Unit Exercises own judgment and is a resource for others. Works independently with assignments often self-initiated 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 ICON is an award-winning workplace that enables you to make a difference to patients’ lives by being part of a world-class clinical research organisation that helps deliver new medicines & medical devices that are benefitting patients worldwide. You are also part of a diverse company that cares about our world and is dedicated to conducting business more sustainably and supporting the communities in which we live. If you’re as driven as we are, join us. You’ll be working in a great environment, with some of the brightest and the friendliest people in the sector, and you’ll be helping shape an industry. Didn’t find the role you were looking for? 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