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Global Clinical Trial Lead
hace 3 semanas
As a Global Clinical Trial Lead, you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.
This position will primarily support the Global Program Leaders (GPLs) in managing a Clinical Team to meet the deliverables outlined in the Compound Development Plan (CDP). Responsibilities include understanding the drug development process to deliver a clinical program in accordance with quality, timelines, and budget, in close partnership with the GPL, Clinical Leader, and Project Management Lead (PML) at the Clinical Development Team (CDT) level. You will also manage external partners and non-vendor relationships, oversee stage gate activities for TA governance (such as writing memos and facilitating meetings), liaise with functions responsible for clinical supplies, address Urgent Safety Measures, and support financial and timeline planning.
What you will be doing:
- Manage Clinical Team (CT) agendas, information, documentation, and communications to ensure timely and accurate dissemination of the CT strategy and operational status across the cross-functional team and external partners. Document team meetings, key decisions, actions, risks, and communications.
- Partner with the GPL, GTL, program Coordinators, and Finance to support ongoing forecasting for the clinical program.
- Collaborate with cross-functional leads within Global Development and external departments such as regulatory, finance, clinical supplies, biomarker, and Global Medical Safety to ensure effective communication, escalation, and resolution of risks and issues related to quality, timelines, and budget.
- Manage governance infrastructure and reporting with co-development and external partners as directed by the GPL.
- Oversee clinical team governance deliverables, partnering with GTLs for trial-level information.
What you need to have:
- Bachelor’s Degree or equivalent work experience; Post-Graduate degree in Project Management or Business is preferred.
- Professional Project Management certification is preferred.
- At least 5 years of industry/CRO/business experience in clinical drug development and/or clinical operations; clinical R&D experience is a plus.
- Minimum of 3 years’ experience in Project Management.
- Experience leading cross-functional global teams is required.
- Ability to resolve conflicts and influence teams without direct authority.
- Experience in planning and managing governance processes.
- Proficiency in MS Project is required.
What ICON can offer you:
Our success depends on our people. We prioritize building a diverse culture that rewards high performance and nurtures talent. Besides a competitive salary, ICON offers benefits focused on well-being and work-life balance, including various leave entitlements, health insurance, retirement plans, 24/7 Employee Assistance Program, life assurance, and flexible country-specific benefits such as childcare vouchers, gym discounts, and travel passes.
Visit our careers website to learn more about working at ICON:
At ICON, inclusion & 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 without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or veteran status. If you require a reasonable accommodation during the application process or to perform essential job functions, please let us know through the provided form:
We encourage you to apply even if you don’t meet all requirements — you might be exactly who we’re looking for
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