Technical Project Manager - IRT
On-site · Dublin, Leinster, Ireland or Reading, England, United Kingdom
Job Summary
Lead end-to-end planning, design, and implementation of IRT/RTSM systems for clinical trials, including integration with broader clinical ecosystems. Define project scope, requirements, and deliverables in collaboration with clinical and technical stakeholders; oversee IRT system configuration, testing (UAT), and deployment readiness; coordinate with vendors for build, validation, and ongoing maintenance; ensure data flow and regulatory compliance (GxP, 21 CFR Part 11) across systems (IRT–EDC, IRT–CTMS, etc.); monitor progress, budgets, risks, and performance; drive continuous improvement of IRT delivery processes. Strong cross-functional collaboration, communication to executive leadership, and a solid foundation in clinical trial processes and data integration.
Required Qualifications
- Bachelor’s degree in Information Technology, Life Sciences, Project Management, or a related field
- 3–5 years of project management experience in a technical environment, preferably within clinical research, pharmaceuticals, or CRO settings
- Proven experience with IRT/RTSM systems in clinical trials, including system implementation, configuration oversight, and vendor management
- Familiarity with clinical trial system integrations (e.g., IRT–EDC, IRT–CTMS) and data flows across the clinical technology landscape
- Strong understanding of clinical trial processes including randomization, drug supply management, and patient tracking
- Experience with project management methodologies (Agile, Waterfall, or hybrid) and tools
- Demonstrated ability to manage multiple projects simultaneously with strong organizational, analytical, and problem-solving skills
- Excellent communication and stakeholder management skills, with the ability to translate complex technical concepts to non-technical audiences
- Knowledge of regulatory and compliance requirements in clinical systems (preferred)
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