- Legend Biotech USA, Inc. (Raritan, NJ)
- …of an immunotherapy in the treatment of multiple myeloma.Legend Biotech is seeking Associate Director, Engineering as part of the Technical Operations team based in ... Raritan, NJ. Role OverviewThe Associate Director of Engineering is a strategic and operational...and systems support business goals and comply with safety, regulatory , and sustainability standards. This position is a key… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …areas centered around rare diseases and immune disorders. Summary The Associate Director, Global Oncology Medical Affairs, Medical Analytics will be responsible ... to communicate key findings and recommendations to internal stakeholders, including senior leadership and medical affairs teams. Ensure utilization of advanced… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …on the Strategic Pricing and Contracting team. Works closely with senior level partners in field Account Management across channels (Institutional, Rare ... contracts to customers Provides regular updates for Brand Teams and Senior Management on contract performance issues, including over- and under-performing contracts… more
- Coinbase (Trenton, NJ)
- …management processes. *What you'll be doing (ie. job duties):* * The Senior Associate of Regulatory Change Management (RCM) will support the management, ... connection, and alignment. Attendance is expected and fully supported. The Coinbase Regulatory Change Management (RCM) function is responsible for the… more
- Parexel (Trenton, NJ)
- … regulatory requirements and processes to a major, dedicated client partnership. As a Senior Regulatory Affairs Associate , you will serve as the primary ... Bring your expert knowledge of FDA regulatory requirements and guidelines to Parexel! We are...HAs to secure approvals. * Provide local input for change control and post-approval requirements. * Collaborate with global… more
- Otsuka America Pharmaceutical Inc. (Trenton, NJ)
- The Associate Director of Regulatory Intelligence leads the collection and dissemination of regulatory intelligence and collaborates with SMEs to interpret ... the impact of regulatory changes to the pharmaceutical environment. **Job Description** +...coordinate projects. + Demonstrates experience interacting with and supporting senior leadership. + Previous experience with people management and… more
- GRAIL (Trenton, NJ)
- …to project teams and leadership. They may manage and provide direction to regulatory staff and, when required, participate in senior management meetings as ... when it can be cured. We are working to change the trajectory of cancer mortality and bring stakeholders...information, please visit grail.com . The role assists with regulatory strategy and the development of submissions in partnership… more
- Parexel (Trenton, NJ)
- The Senior Clinical Research Associate (SrCRA) has local responsibility for the delivery of the studies at allocated sites and is an active participant in the ... in close collaboration with other CRAs and the Local Study Team/ Local Study Associate Director (LSAD) to ensure that study commitments are achieved in a timely and… more
- AIG (Parsippany, NJ)
- …the way we help customers to manage risk. Join us as a Business Intelligence Senior Delivery Associate to play your part in that transformation. It's an ... critical to ensuring consistent application availability, compliance with internal and regulatory standards and ongoing enhancements of our BI capabilities. You will… more
- Bristol Myers Squibb (Madison, NJ)
- …strategy, analytical methods, specifications, reference standards, stability, investigations, change control, product complaints, and regulatory submissions. ... careers.bms.com/working-with-us . **Position Summary** Bristol-Myers Squibb is seeking an Associate Director, Principal Product Quality Leader (PQL), in Global… more
- Sunrise Senior Living (Bridgewater, NJ)
- **When you join Sunrise Senior Living, you will be able to use your unique skills to empower residents to live longer, healthier, and happier lives. Not only will ... and shed light on meaningful ways to serve, grow, and shine together.** **Sunrise Senior Living was again certified as a Great Place to Work(R) by Activated… more
- Otsuka America Pharmaceutical Inc. (Princeton, NJ)
- …needs and nutraceutical products for the maintenance of everyday health. As an Associate Director, Biostatistician, you will be a champion of Otsuka's culture and ... statistical expertise/input in the drug development including clinical development plan and regulatory submission strategy. This is a strategic and critical role in… more
- Integra LifeSciences (Trenton, NJ)
- …pathways to advance patient outcomes and set new standards of care. The ** Associate Manager, Medical Writing** is a senior level professional with advanced ... Building Careers. Joining us is a chance to do important work that creates change and shapes the future of healthcare. Thinking differently is what we do best.… more
- Otsuka America Pharmaceutical Inc. (Trenton, NJ)
- The Associate Director, Scientific Communications manages the execution of the core scientific and medical communications strategy for the relevant therapeutic area ... consistency, and compliance. This position reports directly to the Senior Director, CNS Medical Communications Lead. **Key Responsibilities Include:** **Global… more
- Otsuka America Pharmaceutical Inc. (Trenton, NJ)
- **Job Summary** The Associate Director, Quality Operations will lead initiatives that drive operational excellence, enhance risk management practices, and optimize ... as well as enhance overall operational alignment. + Ensure effective change management strategies are applied to drive successful implementation and adoption… more
- Otsuka America Pharmaceutical Inc. (Princeton, NJ)
- The Associate Director will serve as a key member of the Learning Center of Excellence within Global Quality, responsible for designing, implementing, and sustaining ... (G&A) functions. This role ensures that learning strategies align with regulatory requirements, corporate standards, and business objectives, fostering a culture of… more
- Humana (Trenton, NJ)
- …transforming how Medicare Advantage is sold, and design is at the heart of that change . As a Senior Product Designer, you'll join a growing digital organization ... trustworthy. This is an opportunity to step into a senior role, work in an agile, fast-moving setting, and...ecosystem + Balance ideal UX with technical feasibility and regulatory requirements, knowing when to push and when to… more
- Otsuka America Pharmaceutical Inc. (Trenton, NJ)
- …to drive alignment of labeling content and strategy. + Partner with Global Regulatory Affairs to ensure that all labeling is aligned with the product global ... all global labeling components. + Represent Global Labeling on product-specific Regulatory and Cross-Functional teams, as appropriate. + Collaborate with global… more
- Humana (Trenton, NJ)
- …part of our caring community and help us put health first** The Associate Director of Cloud Infrastructure Operations is responsible for leading Humana's enterprise ... at the intersection of operations, technology, and AI innovation. The Associate Director of Cloud Infrastructure Operations will drive the evolution of… more
- IQVIA (Parsippany, NJ)
- …environment with evolving priorities, the role ensures high-quality data delivery and regulatory compliance across all phases of the trial. Candidates who will ... trial execution, maintain inspection readiness, and uphold GCP, SOP, and local regulatory standards. **_Two years of clinical trial management experience is required… more
