
Director, Portfolio Strategy – Asset Management
Posted Sep 8

Posted Sep 8
This is a fully remote position, open to applicants in New Jersey.
• Lead the development of cross-functional asset strategies, program planning, and execution in collaboration with R&D and Commercial teams.
• Create unique, reimbursable products that enhance patient lives on a global scale.
• Synchronize development plans, budgets, resources, team priorities, and Action Point stage-gate requirements.
• Formulate essential asset deliverables, including annual objectives, PTRS, TPP, NPV, as well as Development and Commercialization Plans.
• Reevaluate strategies and suggest adjustments based on external market dynamics and evidence.
• Coordinate contributions from global affiliates towards Development and Commercialization Plans.
• Monitor plans, objectives, asset performance metrics, risks, issues, and mitigation strategies.
• Communicate with senior management and facilitate timely resolution of emerging challenges.
• Cultivate cohesive, globally-focused asset teams.
• Manage governance touchpoints, stage gates, asset evaluations, and ensure follow-through.
• Assist in onboarding and mentoring junior asset managers and newer PS&AM staff.
• Drive departmental initiatives and participate in goal setting, forecasting, budget management, and resource allocation.
• Offer guidance on Otsuka processes, global collaboration, and alliance management.
• Prepare reviews for the PS&AM functional business case.
• Develop and uphold standard practices, systems, tools, milestones, metrics, and knowledge repositories.
• Support technical subject matter experts with asset management tools and systems.
• Establish and track OPDC key performance indicators.
• Oversee project management, asset management, and project coordinator roles as required.
• Manage the PS&AM budget, headcount, indirect expenses, and budgetary needs.
• Extensive experience in the drug development process and the interrelationships of individual development activities.
• A minimum of 3 years of managerial or supervisory experience in support of R&D, preferably within drug development (preferred).
• Strong understanding and knowledge of the science, therapeutic area, and commercial landscape relevant to assigned programs.
• Capability to work independently with minimal supervision, as well as in team and cross-functional settings.
• Proven ability to build positive relationships with internal and external business partners and influence others without formal authority.
• Effective communication skills at all organizational levels.
• Keen attention to detail with the ability to maintain a strategic overview.
• Robust decision-making and problem-solving/issue-resolution capabilities.
• Proficient meeting facilitation skills.
• Experience in budget management.
• Bachelor’s degree or higher.
• 10 years of cross-functional Program Management experience in the pharmaceutical or biotech industries, specifically in drug or product development, including managerial experience.
• Comprehensive medical, dental, vision, and prescription drug coverage.
• Company-sponsored basic life insurance.
• Accidental death and dismemberment insurance.
• Short-term and long-term disability insurance.
• Tuition reimbursement.
• Student loan assistance.
• Generous 401(k) matching.
• Flexible time off.
• Paid holidays.
• Paid leave programs.
• Additional company-provided benefits.
• Incentive opportunities.
Headway
Reinsurance Group of America, Incorporated
Regeneron
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