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Niche IRT and clinical trial expertise plus seniority reduces candidate competition.
Highly specialized clinical trial and IRT domain experience limits cross-industry portability.
Requires specific IRT, GCP and regulated clinical experience, creating strict shortlisting filters.
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Translate clinical trial protocols into optimized IRT implementations ensuring accurate randomization, supply management, and regulatory compliance.
Define and manage scoping, requirements gathering, prioritization, and documentation for large, complex clinical trial initiatives.
Identify risks early, drive process improvements, support go-live readiness, and collaborate with cross-functional and external teams for successful global clinical studies.
Proven professional experience in clinical development within life sciences or a very similar Senior Solutions Designer role.
Bachelor's Degree in a technical discipline (Maths, Science, Engineering, Computing) or equivalent project experience.
Deep understanding of IRT platforms, clinical trial design (including adaptive, double-blind studies), and GCP principles.
Experience working in regulated environments (GxP) and familiarity with Agile methodologies; fluent English required.
Experienced in designing and building clinical studies across multiple therapeutic areas and phases with global trial exposure.
Strong capability to manage requirements from diverse stakeholders and influence cross-functional teams in highly regulated environments.
Demonstrated ability to identify risks and implement process improvements in complex clinical trial systems with strong communication and documentation skills.