Senior Director, Global Regulatory Strategy

🕒 vor 8 Tagen

🇺🇸 Vereinigte Staaten – Remote

💵 $230.720 - $345.000 / Jahr

⏰ Vollzeit

🟠 Senior

🚔 Compliance

👻 Geisterscore 0%

Was es bedeutet: wie wahrscheinlich diese Stelle offen bleibt, ohne dass aktiv eingestellt wird.So liest du es: 60 % oder höher heißt, wir halten das für einen Geisterjob. Niedrigere Werte sind weniger bedenklich.Wie wir werten: Dauer offen, Neuveröffentlichungen, offene Stellen vs Teamgröße, wie schnell Stellen geschlossen werden, und ob ein Gehalt angegeben ist.Hinweis: eine Schätzung aus öffentlichen Daten, kein Urteil über das Unternehmen. Echte Stellen können hoch punkten, nutze es also als Hinweis, nicht als Fakt.

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Otsuka Pharmaceutical Companies (U.S.)

WebsiteLinkedInAlle Stellen

1001 - 5000 Mitarbeiter

💊 Pharmazie

🏥 Gesundheitswesen

🧬 Biotechnologie

Pharmaceuticals • Healthcare • Biotechnology

Die Otsuka Pharmaceutical Companies (U. S. ) sind ein bedeutender Akteur in der Pharmaindustrie und widmen sich der Entwicklung innovativer Produkte für eine bessere Gesundheit weltweit. Das Unternehmen besteht aus zwei Hauptgesellschaften: Otsuka America Pharmaceutical, Inc. (OAPI), die auf die Vermarktung von Otsuka-entdeckten und lizenzierten Produkten in Nordamerika spezialisiert ist, und Otsuka Pharmaceutical Development & Commercialization, Inc. (OPDC), die sich auf die klinische Entwicklung und globale Zulassung innovativer Gesundheitslösungen, insbesondere im Bereich der Neurowissenschaften, konzentriert.

Beschreibung

• Provide strategic leadership and oversight for a therapeutic area portfolio of development and marketed products • Lead execution of individual product and portfolio-wide regulatory strategies • Align global regulatory strategy with development priorities and global business objectives • Drive portfolio planning, governance, risk management, and enterprise decision-making • Evaluate benefit-risk profiles, development opportunities, competitive landscapes, and emerging regulatory trends • Identify and manage regulatory risks and opportunities, recommending mitigation strategies and contingency plans • Oversee global regulatory milestones including INDs, CTAs, NDAs, BLAs, MAAs, label expansions, and post-approval submissions • Oversee regulatory planning and execution across multiple programs to ensure timely submissions, approvals, and lifecycle deliverables • Review regulatory positions, critical documents, agency responses, and submission content • Drive global lifecycle management strategies to enhance product value, expand indications, and maintain compliance • Establish and oversee global health authority engagement strategies • Lead high-impact agency interactions, regulatory negotiations, briefing packages, and responses to complex agency questions • Serve as senior regulatory representative on 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 • Lead, develop, and mentor Global Regulatory Leads and regulatory team members • Ensure resource allocation, succession planning, and capability development • Champion accountability, innovation, and operational excellence within the regulatory function • Ensure compliance with global regulations, company policies, and quality standards • Lead initiatives for regulatory effectiveness, operational efficiency, best practices, governance, inspection readiness, and continuous improvement

🎯 Anforderungen

• Advanced degree in a scientific discipline required; PhD, PharmD, MD, or equivalent preferred • Minimum 15 years of progressive regulatory affairs experience within the pharmaceutical or biotechnology industry • Significant experience developing and leading global regulatory strategies across multiple development and commercial programs • Demonstrated success influencing portfolio-level decisions and achieving regulatory approvals in major global markets • Proven track record leading complex health authority interactions, negotiations, and regulatory risk-management activities • Experience leading and developing high-performing regulatory teams and managing organizational priorities • Strong understanding of portfolio governance, strategic planning, and cross-functional drug development processes • Expert knowledge of global drug development, regulatory frameworks, and registration requirements across major markets • Demonstrated ability to develop and execute portfolio-level regulatory strategies in a complex global environment • Strong business acumen balancing regulatory, scientific, operational, and commercial considerations • Expertise in regulatory risk assessment, scenario planning, and strategic decision-making • Exceptional leadership, influencing, negotiation, and stakeholder management skills • Proven ability to operate effectively at executive and governance levels • Strong people leadership capabilities, including organizational development, coaching, and talent management • Excellent communication and presentation skills with experience interacting with senior executives and global health authorities • Ability to lead through complexity, ambiguity, and organizational change while maintaining strategic focus

🏖️ Vorteile

• Comprehensive medical, dental, vision, and prescription drug coverage • Company-provided basic life insurance • Accidental death and dismemberment insurance • Short-term and long-term disability insurance • Tuition reimbursement • Student loan assistance • Generous 401(k) match • Flexible time off • Paid holidays • Paid leave programs • Other company-provided benefits