Manage regional components of a large, complex clinical trial within the inflammation therapeutic area
Independently drive study activities with minimal oversight
Lead cross-functional timelines and ensure alignment across stakeholders
Proactively identify operational risks, escalate issues appropriately, and implement solutions
Support study logistics and operational planning to achieve program milestones
Lead vendor management activities and maintain strong oversight of external partners
Draft and coordinate review of key study documents including protocols, informed consents, monitoring plans, investigator brochures, and clinical study reports
Maintain study timelines and support study budget activities
Requirements
3+ years of clinical project management experience within clinical research
Experience supporting complex Phase 2b clinical studies within the inflammation therapeutic area
Strong vendor management and oversight experience
Demonstrated understanding of the full clinical trial lifecycle from start-up through closeout
Experience managing cross-functional clinical trial activities in a matrixed environment
Ability to independently manage priorities and navigate operational challenges with minimal supervision
Benefits
Health benefits to include Medical, Dental and Vision
Company match 401k
Eligibility to participate in Employee Stock Purchase Plan
Eligibility to earn commissions/bonus based on company and individual performance