Director, Statistical Programming, Clinical Schedules (Hybrid)
Core
Direct clinical schedule managers to develop and review randomization and component ID schedules for drug and vaccine programs across early and late phase development.
Role type
Director, Clinical Schedule Management
Builds
Clinical trial randomization schedules, component ID specifications, and unblinding preparations for medical drugs and vaccines
Domain
Biopharmaceuticals / Clinical Trials
Deliverable
production ML models | product features | dashboards & analysis | research | client delivery | infrastructure | physical/clinical work
Required skills
Organizational Leadership, People Management, Program Delivery Management, Statistical Analysis, Strategic Planning, Stakeholder Relationship Management, Functional Strategy, Item Response Theory (IRT)
Preferred skills
Change Management, Process Improvements, Agile Thinking
Technologies
None explicitly stated
Responsibilities
Direct clinical schedule managers in developing randomization and component ID schedules; Interact with cross-functional teams to evolve clinical schedule management and study blinding capabilities; Set direction for clinical schedule management across therapeutic areas; Manage staff resources and forecast support; Ensure application of SOPs and quality/compliance measures; Engage with stakeholders to solve business challenges; Provide technical guidance; Hire and develop qualified staff; Lead departmental strategic initiatives; Represent Clinical Schedule Management at a leadership level.
Seniority
Director, strategic leadership & team management
