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Associate Director, Study Feasibility

Irvine, CA, us💼 Full-time🗓 2026-09-11 → 2026-09-25

Core

Partner with study teams to assess design feasibility, optimize country/site selection, and provide strategic consultation on protocol, patient burden, and recruitment for global clinical trials.

Role type

Senior IC clinical development operations leader (study feasibility)

Builds

Global Phase 2 and Phase 3 clinical trials

Domain

Pharmaceutical clinical development

Deliverable

production ML models | product features | dashboards & analysis | research | client delivery | infrastructure | physical/clinical work

Required skills

Clinical study design, global strategy facilitation, matrix management, scientific analysis, patient recruitment planning, protocol assessment, site selection, therapeutic area expertise

Preferred skills

Oncology, Neurology, or Immunology background, drug development process knowledge

Technologies

Clinical trial management systems, statistical analysis tools

Responsibilities

Facilitate cross-functional global strategy discussions for operational feasibility, support strategic planning for large-scale global trials, drive analytical insights for study recruitment planning, conduct scientific and operational analyses for study engagements, provide consultation on country strategy and site selection, lead projects to improve team capabilities

Seniority

Senior, hands-on IC with strategic oversight

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