- Daiichi Sankyo, Inc. (Bernards, NJ)
- …rare diseases and immune disorders. SummaryThe Associate Director , Global Medical Affairs (GMA) Oncology- Medical Content and Training works with ... of global scientific and training deliverables. The Associate Director develops and executes Medical Content and Training plans and works closely with… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …other research areas centered around rare diseases and immune disorders. Job Summary: The Associate Director of Regulatory Writing is a key role responsible for ... to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class...and strategic insights at the study team level. The Associate Director of Regulatory Writing must possess… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …other research areas centered around rare diseases and immune disorders.Summary: The Associate Director , Regional Marketing Conventions & Field Programs will be ... to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class...while ensuring adherence to DS policies and procedures. The Associate Director , Regional Marketing Conventions & Field… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …pharmaceutical therapies to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class science and ... with contract manufacturing organizations CMO. This position develops strategy, prepares content templates and leads technical teams in preparation of submission… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …pharmaceutical therapies to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class science and ... Procurement's intranet portal, which includes ongoing management of portal content , recommendations for system improvements, driving innovation, user training, and… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …pharmaceutical therapies to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class science and ... external guidelines, reviewing US and EU package inserts with regard to both content and format. Follows internal processes for record keeping and tracking of… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …both internal and external CMO sitesDrive new process version plans and content for regulatory submissionsEnsure global records are consistent and maintained to ... on race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity or expression, age, disability,… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …of Global RD and PV QA organizational strategy in collaboration with the Associate Director Global Strategy and Operations and Head Global Strategy and ... to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class...Operations. In collaboration with the Associate Director Global Strategy and Operations and… more
- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …diseases and immune disorders. **Summary** The Associate Director , Global Medical Affairs (GMA) Oncology- Medical Content and Training works with ... of global scientific and training deliverables. The Associate Director develops and executes Medical Content and Training plans and works closely with… more
- Bristol Myers Squibb (Princeton, NJ)
- …lives. Read more: careers.bms.com/working-with-us . Employer: Bristol-Myers Squibb Company Position: Associate Medical Director , Eliquis Worldwide Medical ... as functional area lead and scientific point for agency development of medical content for scientific venues including international congresses, advisory boards,… more
- Ascendis Pharma (Princeton, NJ)
- …for employees to grow and develop their skills. The Regulatory Affairs (RA) Associate Director , Labeling will be responsible for labeling activities across ... States and the Americas and supporting global needs as required. The RA Associate Director , Labeling will be overall responsible for ensuring compliance with… more
- J&J Family of Companies (Trenton, NJ)
- Associate Director , Thought Leader Liaison, Neurology Rare Disease - Northeast - 2406207036W **Description** Johnson & Johnson is recruiting for an Associate ... profoundly impact health for humanity. Learn more at https://www.jnj.com/ . The Associate Director Thought Leader Liaison's (TLL) key primary responsibility is… more
- Takeda Pharmaceuticals (Trenton, NJ)
- …in order to bring life-changing therapies to patients worldwide. Join Takeda as Associate Director , Global Labeling Lead where you will be responsible for ... the development and implementation of labeling content and strategy of multiple assigned products in various...at the Labeling cross functional teams including clinical, safety, medical affairs, and commercial, to ensure the highest level… more
- Bristol Myers Squibb (Princeton, NJ)
- …US Medical Information, Global Escalations, WW SRD and Variant Content . **Key Responsibilities** 1. Execute strategy for US customer engagement: Medical ... design, develop, and evolve industry leading Customer Engagement and Medical Information call center capabilities while optimizing the customer experience.… more
- J&J Family of Companies (Titusville, NJ)
- Associate Director , RA Labeling Product Leader (1 of 2) - 2406187352W **Description** Johnson & Johnson Innovative Medicine is recruiting for an Associate ... + Make recommendations and provide advice and guidance about labeling content , processes, timelines, and scientific integrity. Coordinate the resolution of any… more
- Takeda Pharmaceuticals (Trenton, NJ)
- …is true to the best of my knowledge. **Job Description** ** Associate Director , Nonclinical Regulatory Writing and Submission Support,** **_Gastrointestinal ... you will be a vital contributor to our inspiring, bold mission. As an Associate Director in the Nonclinical Regulatory Writing and Systems (NRWS) Department… more
- Bristol Myers Squibb (Princeton, NJ)
- …process with a BMS Global Program Team (GPT) in early and/or late development. The Associate Director PM will provide content expertise to the timing, costs, ... operational lead for development and lifecycle management programs, the Associate Director GPM works to ensure that...plans then in effect and may include the following: Medical , pharmacy, dental and vision care. Wellbeing support such… more
- AbbVie (Branchburg, NJ)
- …@abbvie on Twitter, Facebook, Instagram, YouTube and LinkedIn. Job Description The Associate Director , Clinical Development will have global or regional ... that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a...Lead and Clinical Science Lead and Clinical Scientist. The Associate Director , Clinical Development should expect to… more
- Bristol Myers Squibb (Princeton, NJ)
- …questions regarding drug products. The CMC Regulatory Associate Director , Biologics is responsible for content development, compilation, maintenance, ... participating/leading HA meetings); and/or post-approval submissions. In this role, the GRS-CMC Associate Director , Biologics will serve as the primary interface… more
- J&J Family of Companies (Titusville, NJ)
- Associate Director , North America Regulatory Lead - 2406196976W **Description** Johnson & Johnson Innovative Medicine is recruiting for Associate Director ... potential. At Johnson & Johnson, we all belong. The Associate Director , Regulatory Affairs will be responsible...strategy. + Lead and oversee the preparation of dossier content for INDs, BLA/NDA according to the strategic plan… more
