- Genmab (Plainsboro, NJ)
- …surveillance of new and updated regulations/guidelines and assess the impact on drug safety processes at Genmab. Ensure compliance with regulatory guidelines and ... first human trials; (b) overseeing multiple trials with safety inputs at the global level; (c) international experience with internal and external stakeholders; (d) … more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …across multiple functional areas. Relationships You will report to the Senior Director - Global Regulatory Portfolio Lead. Essential Functions Serve as ... preferred Minimum of 8 years total pharmaceutical/related industry experience in drug development required Demonstrated knowledge of global regulatory… more
- Genmab (Plainsboro, NJ)
- …be our best, and authentic is essential to fulfilling our purpose.The RoleThe Associate Director acts as a statistical expert supporting the clinical development ... as trial responsible statistician with responsibilities as described below. The Associate Director contributes to clinical development strategies and… more
- Genmab (Plainsboro, NJ)
- …best, and authentic is essential to fulfilling our purpose.The Role & DepartmentThe Associate Director , Vendor Management, will play a pivotal role in managing ... new trials to ensure efficient and effective trial operations.Point of Contact for Global Clinical Trial Managers: Act as the primary point of contact, facilitate… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …Nordisk, you will have the opportunity to build a life-changing career in a global business environment. We encourage our employees to make the most of their talent, ... actionable insights to guide the business. Relationships Reports to the Director , MAPA Insights. Internal relationships include close interactions with Market Access… more
- Genmab (Plainsboro, NJ)
- …authentic is essential to fulfilling our purpose.Reports to: Senior Director , Commercialization and Enabling Function Data ProductsJob Type: Full-TimePosition ... Medical Affairs and enabling functions.At Genmab, IT & Digital follows a global , product-based operating model; the PO, Commercial & Enterprise Data Products will… 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 ... or a life sciences/pharmacy nursing degree with 15+ years' experience in global safety surveillance and/or clinical/ drug development Excellent verbal and written… more
- Genmab (Plainsboro, NJ)
- …essential to fulfilling our purpose.The Role & Department As a Senior Programming Associate or Programming Manager, you will be in the Statistical Programming team ... making and reporting to health authorities. You will report to the Director , Programming, and work closely with Data Management, Clinical Programming, Statistics,… more
- Merck & Co. (North Wales, PA)
- …our company's biopharmaceutical business.This position operates under the guidance of the Associate Director who supports the Global Regulatory Affairs ... biopharmaceutical company.- Our Research Laboratories drive break-through science through drug discovery, development, and clinical evaluation to address the… 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 ... 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
- 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
- Organon & Co. (Plymouth Meeting, PA)
- **Job Description** **The Position** The Associate Director , Global Data Steward is responsible for operational data ownership and stewardship for the ... global commercial data and analytics organization, establishing and overseeing...and medical leave, and health benefits including medical, prescription drug , dental, and vision coverage in accordance with the… more
- Merck (Upper Gwynedd, PA)
- …obtain shortest time to approval by global regulatory agencies. + Reports to Associate Vice President, Executive Director , or Senior Director in the ... **Job Description** We are seeking a Director (Principal Scientist), Global Regulatory Affairs...teams for meetings with FDA at any phase of drug development. Lead cross-functional efforts to prepare for advisory… more
- Merck (West Point, PA)
- …Our company is seeking a highly motivated candidate for the position of Director , Vaccine Drug Product Development. Vaccine Drug Product Development ... **Job Description** Our company is a global health care leader with a diversified portfolio...The Director will report to the Executive Director of Vaccine Drug Product Development, have… more
- Takeda Pharmaceuticals (Trenton, NJ)
- …to the best of my knowledge. **Job Description** **About the role:** ** Associate Director , Nonclinical Regulatory Writing and Submission Support,** **_Oncology ... 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
- 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...quality and safety. This position will report to the Global Director , Biosafety and Toxicology, and sit… more
- CSL Behring (King Of Prussia, PA)
- …used to treat serious and often rare conditions. Could you be our next Associate Director , R&D Project Planning Capability Lead? This position is located in ... CSL Behring is a global biotechnology leader, guided by a promise to...Prussia PA office. It is a Hybrid role. The Associate Director , R&D Project Planning Capability Lead,… 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
- Organon & Co. (Plymouth Meeting, PA)
- …This position has accountability for the management of the Regional Biosimilar Accounts Director (RBADs) and Associate Account Executives (AAEs) roles that are ... nimble commercialization approach. We are recruiting for a Region Director , Northeast US Account Management for the Biosimilars Business...live their best lives. We are a $6.5 billion global healthcare company focused on making a world of… more
