Associate Director, Study Feasibility & Clinical Partnerships
Core
Strategic leadership for protocol and site feasibility across the Care Access Site Network and end-to-end lifecycle management of clinical vendor partnerships.
Role type
Senior IC Associate Director (Clinical Feasibility & Vendor Management)
Builds
Feasibility assessments, vendor selection, and operational frameworks for clinical studies
Domain
Clinical research operations / Healthcare services
Deliverable
production ML models | product features | dashboards & analysis | client delivery | infrastructure
Required skills
Clinical trial feasibility assessment, vendor acquisition and performance management, protocol analysis, cross-functional stakeholder management, strategic planning, data-driven decision making, contract negotiation, process optimization, risk management, project management
Preferred skills
Clinical Project Management, site network experience, CRO/sponsor engagement, advanced degree in life sciences/healthcare
Technologies
CTMS, clinical portals, project tracking tools, Google Suite, Microsoft Office Suite
Responsibilities
Lead feasibility assessments of study protocols across the site network; manage vendor sourcing, qualification, onboarding, and performance; mentor Feasibility and Vendor Acquisition Managers; collaborate with Business Development, Finance, and Legal to align strategies; provide decision-ready insights on vendor performance and operational challenges.
Seniority
Senior, hands-on IC with team leadership
