We interpreted Morrisville, PA as Morrisville, PA. Other options include: Morrisville (Greene County), PA
- Novo Nordisk Inc. (Plainsboro, NJ)
- …across multiple functional areas. Relationships You will report to the Senior Director - Global Regulatory Portfolio Lead. Essential Functions ... difference? The Position We are seeking a collaborative and science-driven global regulatory expert who wants to work with innovative investigational medicines.… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …of Medical Information. Assigned staff members of Medical Information (MI) report to the Associate Director . The Associate Director communicates medical ... About the Department The Clinical, Medical and Regulatory (CMR) department at Novo Nordisk is one...pharmacists, nurses, diabetes educators, and other NNI customers. The Associate Director represents MI, Scientific Communications and/or… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …the head of Clinical, medical, Regulatory (CMR) Business Operations, the Associate Director (AD) is responsible for structuring facilitating and monitoring ... About the Department The Clinical, Medical and Regulatory (CMR) department at Novo Nordisk is one...internal stakeholders. In the execution of specific projects, the Associate Director , will be accountable for managing… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …collaborators, as we embark on shaping our future. The Position The Associate Director , HCP Experience has overall strategic and operational responsibility ... Partnerships and Engagement, Customer Experience and Marketing Enablement, Employee Experience, Regulatory , PRB, PSP, FRM, Conventions, Global Marketing, Launch… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …of ensuring successful program execution. Relationships Reports to the Director , Commercial Communications. The position will interact with cross-functional ... all programming is done compliantly, with close partnerships with legal, regulatory , compliance and medical Oversees project budget and accountable for staying… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- … Global Safety Lead(s), Global Safety Lead(s) and Global Safety Scientist(s)/ Associate within Safety Surveillance. Essential Functions Innovation and ... the US East Coast Development Hub comprised of Senior Global Safety Leads, Global Safety Leads and...external stakeholders. Relationships This position will report to Senior Director Safety Surveillance, US East Coast Development Hub. Key… 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 TAU within our Global Regulatory Affairs organization, based remotely. + Partners with the Global Regulatory Lead (GRL) on Global Regulatory… more
- J&J Family of Companies (Trenton, NJ)
- Associate Director , CMC Regulatory ...**Key Responsibilities:** + Provides guidance and expertise to the Global Regulatory Team to develop global ... 2406221330W **Description** Johnson & Johnson is recruiting for an Associate Director , CMC Regulatory Affairs....Authority** + Ensures the CMC development and commercial product regulatory strategy meets global regulatory … more
- Takeda Pharmaceuticals (Trenton, NJ)
- …true to the best of my knowledge. **Job Description** **About the role:** ** Associate Director , Nonclinical Regulatory Writing and Submission Support,** ... vital contributor to our inspiring, bold mission. As an Associate Director in the Nonclinical Regulatory...members (Clinical, Global Patient Safety, Program Management, Global Regulatory , Regulatory Operations, Drug… 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 ... escalates issues to Global Labeling management and the Global Regulatory Lead (GRL) and proposes risk mitigation strategies for assigned products… more
- Takeda Pharmaceuticals (Trenton, NJ)
- …order to bring life-changing therapies to patients worldwide. Join Takeda as an Associate Director , Global Patient Safety Clinical Operations in Cambridge, ... of clinical trial and Pharmacovigilance methodologies including detailed comprehension of global regulatory requirements. + Good cross-cultural understanding and… more
- 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 ... integrate one global compliance program into...their decisions. + Under the direction of the Senior Director , US and Above Market Medical and Market Access C&E… more
- Takeda Pharmaceuticals (Trenton, NJ)
- …lead writer for important regulatory response documents and key components of regulatory submissions. + The Associate Director , Medical Writing is seen ... in order to bring life-changing therapies to patients worldwide. Join Takeda as a Associate Director Medical Writing where you will be responsible for medical… more
- Fujifilm (Trenton, NJ)
- …Genki - will always be our driving force. Whilst working as the Associate Director of Biosafety in our global Quality team, you'll be joining other motivated ... **Overview** As the Associate Director of Biosafety, you will...Director , Biosafety and Toxicology, and sit under the global quality leadership group ( Regulatory , IT, Safety,… more
- Bristol Myers Squibb (Princeton, NJ)
- …work and in their personal lives. Read more: careers.bms.com/working-with-us . Associate Director , Statistical Programming, provides functional expertise and ... of technical solutions for integrating, analyzing and reporting clinical data. Associate Director drives the development and implementation of innovative… more
- Sumitomo Pharma (Trenton, NJ)
- …seeking a dynamic, highly motivated, and experienced individual for the position of ** Associate Director , Strategic Sourcing - R&D and Supply Chain/TOQ.** The ... Sumitomo Pharma Co., Ltd. is a global pharmaceutical company based in Japan with key...Associate Director Strategic Sourcing R&D and Supply… more
- Bristol Myers Squibb (Princeton, NJ)
- …at work and in their personal lives. Read more: careers.bms.com/working-with-us . The Associate Director , Clinical Data Standards is a leadership role with ... global development and business partners (medical, development, commercial, regulatory & quality etc.). + Influential leadership and communication capabilities… more
- Church & Dwight Co., Inc. (Princeton, NJ)
- …biggest impact because: Together We Have the Power to Win. Role Summary The Associate Director of R&D Technology Development is responsible for guiding and ... advancing our global technology innovation initiatives for our Personal Care and...findings to various teams including technical, marketing, legal, and regulatory . + Act as the main liaison for external… more
- Bristol Myers Squibb (Princeton, NJ)
- …by leveraging internal and external best practices and exploring technologies. The Associate Director (AD), Informed Consent Management role reports to the ... Informed Consent (IC) Management function at BMS sits within Global Development Operations (GDO) and is responsible for managing... Director of Informed Consent Management. The AD will be… more
- Bristol Myers Squibb (Princeton, NJ)
- …at work and in their personal lives. Read more: careers.bms.com/working-with-us . The Associate Director , Media Category Lead is responsible for development of a ... robust global category strategy aligned to achieving dynamic business outcomes....contact for Commercialization-related procurement needs. This will require the Associate Director Procurement Media to have strong… more
