Director of Program Operations leading complex Clinical Trial Management programs. Overseeing clinical operations within timelines, quality, and budgets for clinical research studies.
Responsibilities
responsible for leadership and overall strategic management of one or more complex programs in Clinical Trial Management (CTM)
responsible for clinical operations activities and decisions including quality, timelines and budgets related to the conduct of clinical research studies
interacts with senior level management, external vendors, collaboration partners and clinical study personnel
maintain an overview of clinical program(s) status and issues and proactively communicates progress, risks, issues or changes that may impact quality, timelines and/or budget
provide operational insight into feasibility, timeline and cost estimates during clinical program/study development
oversee clinical study timelines within a clinical program(s)
Requirements
A Bachelor’s degree
minimum of 12 years relevant in-house sponsor-side industry experience
8 years within clinical operations
Benefits
health and wellness programs (including medical, dental, vision, life, and disability insurance)
fitness centers
401(k) company match
family support benefits
equity awards
annual bonuses
paid time off
paid leaves (e.g., military and parental leave)
Job title
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