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Senior Director, Companion Diagnostics in Edison, NJ at DSI

Date Posted: 11/28/2018

Job Snapshot

Job Description

Job Summary:
The primary responsibilities of this position are to lead CDx project teams independently, contribute to strategic decisions for projects w/ a CDx component, collaborate very actively with leadership from other DS functions (Regulatory, Commercial, QA, IPTs, etc) to execute CDx strategies, contribute to due diligence/licensing decisions with a CDx component and represent GCDxC in KOL & CDx regulatory interactions

Responsibilities:
Lead CDx project teams in all areas of CDx development, registration, and commercialization independently
Leads CDx Partner evaluation and selection activities independently
Participates in cross-functional strategic decisions involving CDx. Contributes to global and regional strategic decisions
May independently write publications & regulatory documents
May be responsible for performance management and development of direct reports and department
Represents GCDxC in KOL and global CDx regulatory interactions. Leads KOL & regulatory interactions for programs with CDx component
Participates in due diligence activities

Education:
Experience:

MD, PhD, or PharmD with 8+ years industry experience
Or equivalent experience
People management experience (for managerial track)