- Bristol Myers Squibb (Princeton, NJ)
- …Lead , this role partners with senior leaders across Legal, Commercial, Medical, R&D, Global Drug Development, Regulatory, IT, Audit, Finance and HR to build and ... compliance program into the Worldwide Medical, R&D and Global Drug Development Organizations . In this...their decisions. + Under the direction of the Senior Director , US and Above Market Medical and Market Access… more
- Bristol Myers Squibb (Princeton, NJ)
- …a BMS Global Program Team (GPT) in early and/or late development. The Associate Director PM will provide content expertise to the timing, costs, and ... partner and operational lead for development and lifecycle management programs, the Associate Director GPM works to ensure that cross-functional teams operate… more
- Takeda Pharmaceuticals (Trenton, NJ)
- …company that will inspire you and empower you to shine? Join us as an Associate Director , Global Regulatory Project Management and Strategic Planning - GI2 ... high performance teams and mentoring colleagues. + Significant experience in global drug development regulations, regulatory submissions, lifecycle management,… more
- Takeda Pharmaceuticals (Trenton, NJ)
- …possible in order to bring life-changing therapies to patients worldwide. Join Takeda as Associate Director , Global Labeling Lead where you will be ... of labeling content and strategy of multiple assigned products in various stages of drug development, which may include one high complexity product and updates to or… more
- Bristol Myers Squibb (New Brunswick, NJ)
- …and in their personal lives. Read more: careers.bms.com/working-with-us . **Position Summary** **The Associate Director - Site Planning Global Process Leader ... User Adoption and Sustainability).** **Establish seamless collaboration with other functional global process leaders, the center of excellence, IT and functional… more
- Bristol Myers Squibb (Princeton, NJ)
- …lives. Read more: careers.bms.com/working-with-us . **Position Responsibilities** + Develop global and/or US regulatory strategy for Oncology products in development ... direction and provide leadership for all regulatory interactions with FDA/ global regulatory authorities + Lead regulatory dossier submissions to...and guidelines as they apply to US FDA for drug development and approval. + Expert understanding of … more
- Regeneron Pharmaceuticals (Basking Ridge, NJ)
- We are seeking an Associate Director to join out Oncology Clinical Development department. The Associate Director Clinical Sciences leads in the ... of study data of a clinical development program. The Associate Director leads in a matrix environment...other departments; Member of the Clinical Study Team and Global Clinical SubTeam + Maintains proficient understanding of therapeutic… more
- Bristol Myers Squibb (Princeton, NJ)
- …address external questions regarding drug products. The CMC Regulatory Associate Director , Biologics is responsible for content development, compilation, ... Sciences (GRS) and Global Product and Supply (GPS). The GRS-CMC Associate Director , Biologics will assess Manufacturing Change Controls for global… more
- Ascendis Pharma (Princeton, NJ)
- …and the Americas and supporting global needs as required. The RA Associate Director , Labeling will be overall responsible for ensuring compliance with US ... Ascendis Pharma is a dynamic, fast-growing global biopharmaceutical company with locations in Denmark, Europe,...grow and develop their skills. The Regulatory Affairs (RA) Associate Director , Labeling will be responsible for… more
- J&J Family of Companies (Titusville, NJ)
- Associate Director , Temperature Strategy & Execution - 2406177829W **Description** Johnson & Johnson Innovative Medicine Research & Development (JJIM R&D), part ... of the Johnson & Johnson Family of Companies, is recruiting for an Associate Director , Temperature Strategy & Execution within Clinical Supply Chain (CSC). The… more
- Bristol Myers Squibb (Princeton, NJ)
- …at work and in their personal lives. Read more: careers.bms.com/working-with-us . Associate Director , TA (Therapeutic Area) Analysis Standards Leader is ... across the TA, aligning cross-functionally and driving end to end standards. Associate Director , TA Analysis Standards Leader, independently leads improvement… more
- Bristol Myers Squibb (New Brunswick, NJ)
- …in their personal lives. Read more: careers.bms.com/working-with-us . **Position Summary** The Associate Director Global Delivery Excellence Data and ... strategies for Transportation, Logistics, Distribution, and all other aspects of global drug delivery. + Lead the application of data and technologies including… more
- J&J Family of Companies (Titusville, NJ)
- Associate Director , Capabilities & Deployment, XTA - 2406207093W **Description** Johnson & Johnson is recruiting for an Associate Director , Capabilities ... potential. At Johnson & Johnson, we all belong. The Associate Director , Capabilities & Deployment - XTA,...individual will play a leadership role in harmonization and global standardization within the Delivery Unit's in partnership with… more
- J&J Family of Companies (Titusville, NJ)
- …Johnson & Johnson Innovative Medicine is recruiting for Associate Director , North America Regulatory Lead in Global Regulatory Affairs, supporting ... Associate Director , North America Regulatory Lead...product-related teams. + Provides regional regulatory input to the Global Regulatory Team (GRT) and may participate in the… more
- Taiho Oncology (Princeton, NJ)
- Associate Director , Regulatory Affairs Operations Pleasanton, CA, USA * Princeton, NJ, USA Req #386 Tuesday, August 20, 2024 Looking for a chance to make a ... we earn and maintain the confidence of patients, the global healthcare community, collaborators and partners, and each other....and expanding mid-size oncology company in the role of Associate Director , Regulatory Affairs Operations where you… more
- Bristol Myers Squibb (Princeton, NJ)
- …centralized monitoring for trials across the BMS Research & Development portfolio. The Associate Director , External Data Acquisition is a leadership role with ... and in their personal lives. Read more: careers.bms.com/working-with-us . Global Data Management (GDM) is responsible for clinical trial...the BMS R&D pipeline. This role reports to the Director , External Data Acquisition within GDM and is a… more
- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …other research areas centered around rare diseases and immune disorders. **Summary:** The Associate Director will lead the execution and lifecycle management of ... for cardiovascular diseases, under the Group's 2025 Vision to become a " Global Pharma Innovator with Competitive Advantage in Oncology," Daiichi Sankyo is primarily… more
- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …research areas centered around rare diseases and immune disorders. **Job Summary:** The Associate Director of Regulatory Writing is a key role responsible for ... diseases, under the Group's 2025 Vision to become a " Global Pharma Innovator with Competitive Advantage in Oncology," Daiichi...and strategic insights at the study team level. The Associate Director of Regulatory Writing must possess… more
- System One (Basking Ridge, NJ)
- Job Title: Associate Director , Biostatistics Client: Global Pharmaceutical Company Location: Remote, US Based only - must reside in EST or CST time zones ... document. May participate in meeting or teleconferences with Health Authorities Global BDO Strategy to Improve Drug Development: Primarily participates… more
- Ascendis Pharma (Princeton, NJ)
- …offer a dynamic workplace for employees to grow and develop their skills. The Associate Director Patient Services will be responsible for assisting and managing ... Ascendis Pharma is a dynamic, fast-growing global biopharmaceutical company with locations in Denmark, Europe,...of Patients, Science, and Passion, we use our TransCon(R) drug development platform to fulfill our mission of developing… more