Associate Director, Clinical Portfolio Technology
Core
Shape, deliver, and improve technology capabilities supporting clinical trial execution, study oversight, and portfolio decision-making in a regulated life sciences environment.
Role type
Associate Director, Clinical Portfolio Technology
Builds
Technology plans, roadmaps, and scalable solutions for clinical development and portfolio management
Domain
Life Sciences / Clinical Development / Regulated Technology
Deliverable
production ML models | product features | dashboards & analysis | infrastructure
Required skills
Clinical trial technology knowledge, GxP compliance (21 CFR Part 11, EU Annex 11), vendor management, cross-functional stakeholder engagement, lifecycle management of clinical platforms, data-driven decision-making support, operational process improvement
Preferred skills
Experience with Medidata, SAS, Veeva Vault, CTMS, EDC, RBQM, Agile delivery, AI-enabled capabilities evaluation
Technologies
Medidata, SAS, R/Posit, Veeva Vault, Elluminate, CTMS, EDC, eCOA, eTMF, RBQM
Responsibilities
Drive delivery and adoption of technology capabilities for clinical trial execution and portfolio analytics; Partner with stakeholders to translate business priorities into technology plans and roadmaps; Manage requirements, scope, and release readiness for clinical technology initiatives; Ensure solutions are compliant, validated, and inspection-ready; Identify opportunities to simplify processes and enhance user experience across clinical systems
Seniority
Senior, hands-on IC with strategic planning
