- Otsuka America Pharmaceutical Inc. (Princeton, NJ)
- …+ Drive the development of standardized global training curricula covering scientific exchange, regulatory compliance, data interpretation, and stakeholder ... **Job Summary** The Director , Global Medical Training & Field Excellence will...training programs and field excellence initiatives across Global Medical Affairs . This role is responsible for building capabilities, driving… more
- Otsuka America Pharmaceutical Inc. (Princeton, NJ)
- …but not limited to Translational Research & Biomarkers, Clinical Management, Global Regulatory Affairs , Global Clinical Development (late phase), Data & ... on the early development CNS portfolio and Early Development Teams. This Senior Director is a strategic scientific and clinical leader accountable for the… more
- Sanofi Group (Morristown, NJ)
- **Job Title:** US Medical Director , Dermatology (NextGen Immunology) **Location** : Cambridge, MA Morristown, NJ **About the Job** A strategic medical leadership ... role within Sanofi's Next Gen Immunology Medical Affairs organization, driving evidence-based medical strategy in dermatology and rheumatology therapeutic areas.… more
- Bristol Myers Squibb (Princeton, NJ)
- …and in their personal lives. Read more: careers.bms.com/working-with-us . The Senior Director for Milvexian Global Medical Strategy will provide deep disease state ... focus on strategy, planning, development, and implementation of the medical plan. The Director will report to the Executive Director , Thrombosis Disease Area… more
- Merck (Rahway, NJ)
- …Work closely with a cross-functional group of experts in commercialization, regulatory affairs , statistics, and manufacturing to manage clinical development ... including development strategy, study design, initiation, execution, monitoring, analysis, regulatory reporting, and publication. **Specifically, the Senior Director… more
- Otsuka America Pharmaceutical Inc. (Trenton, NJ)
- …including INDs, IBs, clinical study reports, and NDAs/BLAs. + Collaborate with regulatory affairs on interactions with global health authorities. + Provides ... with emphasis on the large global clinical trials and regulatory filing activities. The Senior Director , GCD...programs after proof of concept through late-stage trials and regulatory submissions. + Provide medical and scientific … more
- J&J Family of Companies (Titusville, NJ)
- …Organization, Finance and Procurement, Global Commercial Strategic Organization, Global Medical Affairs , Regulatory Affairs , Research & Development, Global ... CAPLYTA(R) medical team to support our growing impact in psychiatry. The Director , Program Management (PM) is primarily responsible for leading the program… more
- Bristol Myers Squibb (Princeton, NJ)
- …their personal lives. Read more: careers.bms.com/working-with-us . **Position Summary:** The Director for Admilparant will provide deep disease state knowledge in ... strategy, planning, development, and implementation of the US/Global medical plan. The Director will report to the Senior Director , Admilparant Medical Program… more
- J&J Family of Companies (Titusville, NJ)
- …numbers, your applications will be considered as a single submission. **Purpose:** The Director of Regulatory Medical Writing (RegMW) is recognized as a leader ... developing internal medical writers, and ensuring adherence to best practices and regulatory guidelines. The Director , RegMW has the authority to oversee… more
- J&J Family of Companies (Raritan, NJ)
- …Market Surveillance, Clinical Affairs , Design Quality Engineers, R&D, and Regulatory Affairs relating to literature search and systematic review processes. ... https://www.jnj.com/medtech We are searching for the best talent for an **Associate Director , Medical Writing & Literature Services** . _Remote work options may be… more