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Senior Director, Global Regulatory Strategy

Job in Moscow, Latah County, Idaho, 83843, USA
Listing for: Otsuka America Pharmaceutical Inc.
Full Time position
Listed on 2026-10-03
Job specializations:
  • Management
    Regulatory Compliance Specialist
Salary/Wage Range or Industry Benchmark: 231000 - 345000 USD Yearly USD 231000.00 345000.00 YEAR
Job Description & How to Apply Below

Remote

Full time

R12948

Position Summary

The Senior Director, Global Regulatory Strategy is a senior regulatory executive responsible for providing strategic leadership and oversight for a therapeutic area portfolio of development and marketed products. This role is responsible for leading execution of individual products and portfolio-wide regulatory strategies that enable efficient product development, successful global registrations, and maximized asset value throughout the product lifecycle.

As a member of the Global Regulatory Leadership Team, the Senior Director serves as the regulatory leader for portfolio planning, governance, and risk management activities, ensuring alignment between global regulatory strategy, development priorities, and global business objectives by driving enterprise decision-making, optimizing regulatory pathways, and proactively manage portfolio risks, while building organizational regulatory capabilities.

Key Responsibilities Regulatory Strategy and Portfolio Leadership
  • Provide strategic leadership for assets in a therapeutic area portfolio, ensuring global regulatory strategies are appropriate across development, registration, commercialization, and lifecycle management activities.
  • Support with establishing an integrated regulatory vision and long-term strategy that supports portfolio objectives, optimizes development pathways, and maximizes each products value globally.
  • Drive individual asset and portfolio-level regulatory decision-making by evaluating benefit-risk profiles, development opportunities, competitive landscapes, and emerging regulatory trends.
  • Identify, assess, and proactively manage regulatory risks and opportunities across assets in the portfolio, recommending mitigation strategies and contingency plans.
  • Ensure appropriate regulatory positions, messaging, and strategic approaches across multiple programs and regions to ensure products with the portfolio align with business objectives.
  • Incorporate regulatory intelligence, health authority precedents, and evolving global requirements into portfolio strategy and investment decisions.
Regulatory Submissions and Lifecycle Management
  • Provide strategic oversight for major global regulatory milestones, including INDs, CTAs, NDAs, BLAs, MAAs, label expansions, and significant post-approval submissions.
  • Ensure regulatory submission strategies support overall asset and portfolio objectives and are aligned with global development plans.
  • Oversee regulatory planning and execution across multiple programs to ensure timely submissions, approvals, and lifecycle deliverables.
  • Guide development of regulatory positions and review critical regulatory documents, agency responses, and submission content for strategic alignment and quality for all submissions
  • Drive global lifecycle management strategies that enhance product value, expand indications, and maintain regulatory compliance.
Health Authority Interactions
  • Establish and oversee global health authority engagement strategies across the therapeutic area portfolio.
  • Lead high-impact agency interactions involving significant regulatory, scientific, or business implications.
  • Serve as the senior regulatory advisor for meetings with global regulatory authorities.
  • Provide strategic direction for briefing packages, regulatory negotiations, and responses to complex agency questions.
  • Foster productive relationships with health authorities to facilitate successful development and registration outcomes.
Cross-Functional and Organizational Leadership
  • Serve as the senior regulatory representative on therapeutic area portfolio governance committees, development leadership teams, and strategic planning forums.
  • Partner with Clinical Development, Medical Affairs, Regulatory CMC, Quality, Safety, Commercial, Market Access, and Program Leadership to drive integrated decision-making.
  • Serve as a Global Regulatory lead as well as leading, developing, and mentoring other Global Regulatory Leads and regulatory team members, creating a high-performing and collaborative regulatory organization.
  • Ensure appropriate resource allocation, succession planning, and capability development across the therapeutic area.
  • Provide regulatory expertise and recommendations to support enterprise decision-making .
  • Champion a culture of accountability, innovation, and operational excellence within the regulatory function.
Compliance and Continuous Improvement
  • Ensure regulatory activities are conducted in compliance with applicable global regulations, company…
Position Requirements
10+ Years work experience
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