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Manages Phase I-IV clinical trials (local/regional/global) for a global CRO, overseeing technical, financial, and operational aspects to ensure on-time, on-budget delivery while aligning with regulatory standards and client expectations.
The Project Manager oversees the end-to-end coordination of clinical trials, managing technical, financial, and operational aspects to ensure project deliverables meet quality and timeline expectations. This role requires specific experience in oncology studies and proficiency in clinical trial management systems.
Who we are We’re a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world’s most persistent diseases is not paved by those who play it safe. It is built by those who…
Data Product Analyst builds and governs clinical data assets as high-quality products, ensuring reliability and scalability for AI and analytics systems in a regulated life-sciences CRO.
Design and refine multi-step prompts for AI tools like Claude and Copilot to streamline commercial workflows in a healthcare CRO, building reusable prompt libraries and training non-technical teams.
Develop, test, and maintain SAS programs and clinical databases for drug trials, ensuring data accuracy and compliance with CDISC standards.
Build and maintain clinical trial databases using SAS and CDISC standards, configure eDC systems, and validate data for life-saving medical research.
Design and refine multi-step prompts for AI tools like Claude and Copilot to streamline commercial workflows such as proposals, pricing, and client-facing materials in a healthcare CRO.
Designs and leads global IT infrastructure projects, including cloud, security, and enterprise systems like VMWare, Citrix, and Active Directory, to support a clinical research organization.
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