Director of Program Operations leading strategic management of clinical trial programs at Regeneron. Responsible for overseeing clinical research activities in adherence to regulations and quality standards.
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 in accordance with applicable regulations, ICH/GCP regulations and company Standard Operating Procedures (SOPs) within assigned program(s)
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 clinical program level updates to stakeholders as requested
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) for eligible employees at all levels!
Job title
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