Senior Director, LCM Program Management
About The Position
The Senior Director, Life Cycle Management (LCM) Program Management is a strategic leadership role responsible for governing and driving the end-to-end life cycle management strategy for the lorundrostat program. This leader partners closely with Clinical Development, Regulatory, CMC, Commercial, Medical Affairs, Finance, and Corporate Leadership to ensure that life cycle opportunities are prioritized, and executed. The Senior Director serves as the enterprise LCM orchestrator, translating Corporate strategy into integrated, executable life cycle plans, establishing fit-for‑-‑purpose governance, and enabling data-driven decision making at the GPT and Executive levels. This role requires comfort operating in ambiguity, influencing without authority, and balancing near-term execution with long-term value creation in a rapidly evolving setting.
Requirements
- Collaborative leader who can align diverse stakeholders toward common goals
- Strategic and systems thinking with a portfolio mindset
- Executive presence and exceptional communication skills
- Ability to translate strategy into actionable, integrated plans and pivot, re-evaluate as needed
- Strong risk management, scenario planning, and problem-solving capabilities
- Ability to work under time pressure and effectively in a team or matrix environment
- Metrics-oriented, execution that delivers value and moves the business
- Bachelor’s degree required; advanced degree (MBA, MS, MD, PhD) preferred.
- Extensive experience in program and portfolio management within biopharmaceutical or life sciences organizations.
- Demonstrated leadership across full product life cycle, including launch, and post approval optimization.
- Proven ability to operate at the enterprise and executive level, influencing strategy and decisions across functions.
- Strong track record of leading complex, cross-functional initiatives in fast paced, ambiguous environments.
Responsibilities
- Serve as the Program Management Lead for life cycle initiatives, coordinating cross-functional teams across Clinical Development, Regulatory, CMC, Commercial, Medical Affairs, Market Access, Safety, Quality, and Operations.
- Evaluate, and prioritize life cycle opportunities, risks, and trade-offs aligned with corporate strategy and value creation goals.
- Drive alignment on objectives, scope, timelines, dependencies, and critical path activities across life cycle workstreams.
- Facilitate and lead cross-functional forums, life cycle reviews, and governance discussions to enable timely, well-informed decision making.
- Develop high-quality executive-level materials, dashboards, and decision frameworks that synthesize complex cross-functional inputs.
Benefits
- Position eligible for standard Company benefits including medical, dental, vision, time off and 401K, as well as participating in Mineralys incentive plans are contingent on achievement of personal and company performance.
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What This Job Offers
Job Type
Full-time
Career Level
Director
