- Bristol Myers Squibb (Princeton, NJ)
- …in their personal lives. Read more: careers.bms.com/working-with-us . The Associate Director , Global Supplier Human Rights, is responsible for implementing the ... Chain Human Rights Due Diligence Program for the Procurement organization. This Associate Director will help create key program components and be responsible for the… more
- Bristol Myers Squibb (Princeton, NJ)
- …Read more: careers.bms.com/working-with-us . **Position Summary** The TAIP TA Lead is a senior leadership role reporting directly to the Head of the TAIP unit within ... and Planning (TAIP) organization-an internal consulting team that drives clinical development excellence through data-driven insights, feasibility modelling, and… more
- Bristol Myers Squibb (Princeton, NJ)
- …advocating for BMS's position externally. As part of the team, the Associate Director Regulatory Policy brings an expertise in regulatory affairs and related policy. ... The Associate Director , Regulatory Policy is responsible for driving regulatory policy...stakeholders. + **Project Oversight & Performance Tracking** : Support senior leadership in coordinating and executing major projects (such… more
- Bristol Myers Squibb (Princeton, NJ)
- …work and in their personal lives. Read more: careers.bms.com/working-with-us . The Director , HRBP for US Sales & RDC Capabilities provides strategic people ... partnership to senior leaders across our US Sales organizations. Additionally, this...may be available. The starting pay rate takes into account characteristics of the job, such as required skills,… more
- Bristol Myers Squibb (Princeton, NJ)
- …management through a combination of quantitative and qualitative assessments. The Senior Manager/Associate Director , Portfolio Analytics position will play an ... preferred. + Broad understanding of pharmaceutical industry R&D, including clinical development, regulatory strategy, and competitive dynamics required. If you… more
- Otsuka America Pharmaceutical Inc. (Trenton, NJ)
- **Associate Director , Small Molecule Analytical Development** + Lead and oversee phase appropriate method development and optimization for drug substance and drug ... development teams, ensuring all CMC considerations are accounted for in wider clinical development plans. + Serve as early-stage CMC representative of the department… more
- Gilead Sciences, Inc. (Parsippany, NJ)
- …regulatory requirements; relevant Gilead policies and procedures supporting audits and clinical activities. + Evaluate SOPs, other procedures, data and reporting of ... Audit Heads for Audit related CAPAs. + Stay current with evolving global clinical regulations and guidance. + Support the development of GCP Audit material/insights… more
- Bristol Myers Squibb (Princeton, NJ)
- …. **Position Summary** The TAIP Insights & Innovation (I&I) Lead is a senior leadership role within Bristol Myers Squibb's Trial Analytics, Insights, and Planning ... (TAIP) organization - an internal consulting team that accelerates clinical development through advanced analytics, innovation, and strategic resource planning. As… more
- Otsuka America Pharmaceutical Inc. (Trenton, NJ)
- **Position Summary** The Director , Early Commercial Planning is responsible for supporting early-stage commercialization efforts, ensuring that Otsuka's pipeline ... knowledge of the pharmaceutical research and development process including clinical trial design and evidence generation concepts. + Cross-functional leadership… more
- Bristol Myers Squibb (Princeton, NJ)
- …. **Description** : In support of Commercialization Strategy, the Associate Director of US Predictive Customer Engagement team develops and delivers analytical ... meet the needs of our stakeholders + Engagements with senior leadership of our cross functional stakeholders to deliver...(based on eligibility). The starting pay rate takes into account characteristics of the job, such as required skills… more