About the role

Role: Senior Director of Program Management overseeing Viking's drug programs in metabolic and endocrine disorders, focusing on planning, execution, and cross-functional integration. The role emphasizes leading programs through regulatory milestones (IND & NDA) and influencing cross-functional teams in a fast-paced environment. Responsibilitiesdeveloping and maintaining integrated program schedules managing timelines, risks, and budgets providing decision‑making reports to leadership RequirementsBachelor's in Life Sciences 12+ years in biopharmaceutical drug development with at least 7 years managing clinical‑stage programs experience leading Phase 1–3 programs through major regulatory submissions PMP certification preferred High-Value:expertise in cardiometabolic or endocrine therapeutics GxP and regulatory compliance program budget and risk management cross‑functional collaboration Work setup and travel details are not specified.

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JOB OVERVIEW

Experience level

Manager

Location

San Diego, CA

Occupation

Project Management Specialists

Industry

Research and Development in Biotechnology (except Nanobiotechnology)

Posted

2 days ago

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