Manage PV Operations including intake, case workflow, and personnel oversight. Ensure compliance with regulations, train staff, and collaborate across departments.

The Director of Global Market Research at Otsuka Pharmaceuticals leads market research initiatives for CNS assets, collaborating with cross-functional teams to provide insights for brand development and strategy.

The Workplace Experience Coordinator ensures a productive office environment through operations management, vendor oversight, event coordination, and compliance efforts.

Lead the Quality Management team, ensuring compliance and quality of commercial products through strategies, systems, audits, and reports while managing supplier quality and cross-functional collaborations.

Lead the evolution of external content management to centralized model, manage vendor relationships, develop efficient processes, and ensure compliance with regulations.

As Associate Director, Value and Access Strategy, lead market access strategies, engage with stakeholders, and ensure product differentiation and reimbursement strategies for Otsuka’s portfolio.

Provide analytical support for customs and trade compliance, including monitoring import/export shipments, responding to broker inquiries, and assisting with compliance documentation and recordkeeping.

The Senior Manager supports Global PV compliance through audits, CAPA management, and collaboration with stakeholders to uphold regulatory standards.

The Director of Commercial Data Science will lead data analysis to enhance brand performance and market strategies in nephrology. He/she will collaborate with various teams to implement data-driven insights into business strategies and manage vendor relationships for quality market insights.

The Manager of Product Quality Complaints oversees the complaint management system, ensuring regulatory compliance in handling product complaints and coordinating with various departments. Responsibilities include monitoring product trends, preparing reports, and training staff on complaint resolution.

The Senior Analyst provides customized information strategies and conducts advanced research to support business decisions in various aspects of clinical and commercial development, while also managing information resources and training programs.

The Director will lead product communications strategies for marketed products and pipeline candidates, manage a PR agency, and work cross-functionally for integrated messaging.

The Senior Manager oversees supplier catalogs in SAP Ariba, ensuring data accuracy, compliance, and collaboration with suppliers to optimize procurement processes.

The Director of Corporate Counsel provides legal guidance on employment law, manages litigation, collaborates with leadership, and develops strategies to mitigate risks in compliance with laws affecting corporate operations.

The role involves strategic oversight of HCP engagement operations, managing contracting and payments, ensuring compliance, and working with internal and external stakeholders to enhance transparency and efficiency.

The Ecosystem Lead will develop and execute customer engagement strategies, manage a team of HSAs, and ensure patient-centric solutions while fostering a collaborative culture.

Manage supplier quality assurance and compliance through audits, corrective actions, and quality policy development. Support supplier management and maintain documentation for GMP compliance.

The Manager will ensure compliance with financial transparency laws, oversee report preparation, collaborate with stakeholders, and manage data integrity processes.

The Associate Director, Promotion Compliance reviews and approves promotional labeling for pharmaceuticals, ensuring compliance with regulations and training others on relevant practices.

The Director of Quantitative Pharmacology oversees pharmacometrics activities for drug development, including study design, modeling, and regulatory submissions, leading a team and managing project budgets.