Project Management & Strategic Operations Associate Director
Core
Lead integration and execution of complex pharmaceutical development and regulatory plans for preclinical sciences, ensuring deliverables meet objectives and budget.
Role type
Senior IC program management director (preclinical)
Builds
Integrated project plans, regulatory submissions, and preclinical development programs
Domain
Biotechnology / Pharmaceutical drug discovery and development
Deliverable
production ML models | product features | dashboards & analysis | research | client delivery | infrastructure | physical/clinical work
Required skills
GLP regulations, pharmaceutical drug discovery lifecycle, preclinical regulatory submissions, cross-functional team leadership, budget forecasting, risk management, stakeholder communication
Preferred skills
outsourced preclinical models, IND/CTA and global marketing submissions
Technologies
none stated
Responsibilities
Establish project team operating norms and measure performance; lead teams for critical development projects; review and compile project plans, budgets, and logistics; work with CRO partners on scheduling and reporting; summarize program progress and risk assessments for management; track high-level program deliverables; lead worldwide regulatory submissions from a nonclinical perspective; forecast and maintain program budget; mentor staff and resolve conflicts
Seniority
Director, hands-on IC with people management
