- Genmab (Plainsboro, NJ)
- …to be our best, and authentic is essential to fulfilling our purpose.The RoleThe Global Clinical Trial Manager (GCTM) is accountable for the end-to-end delivery ... of a single or multiple clinical trials from strategy outline through to CSR by...outline through to CSR by leading cross-functional trial specific Clinical Trial Teams (CTT) to deliver clinical … more
- Genmab (Plainsboro, NJ)
- …authentic is essential to fulfilling our purpose.The RoleGenmab is looking for an Associate Director , Global Regulatory Affairs, Regulatory Strategy to be ... a part of our Global Regulatory Affairs organization.In this role, you will work...Global Regulatory Team, Labeling Working Groups, Launch Teams, Clinical Trial Teams, and other cross-functional teams as required… 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 ... About the Department Our East Coast Global Development Hub brings together the best minds...NJ. We support programs from early research through late-stage clinical development. We are building for the future, creating… more
- Genmab (Plainsboro, NJ)
- …to fulfilling our purpose.The RoleThe Global Regulatory Labeling Strategy Sr Manager/ Associate Director will be responsible for leading the development and ... Regulatory Affairs (GRA) and will report to the Sr Director , Labeling, Policy and Intelligence. The position will be...global regulations and guidance as they relate to global labelingUnderstanding of clinical development of novel… 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...internal stakeholders. In the execution of specific projects, the Associate Director , will be accountable for managing… more
- Merck & Co. (North Wales, PA)
- …strategic thinking, ability to comprehend and translate complex scientific & clinical data and deliver results working cross-collaboratively and leading without ... leaders, as well as internal stakeholders, including US & Global Marketing, Medical Affairs, and Outcomes Research.Our US marketing...will report to the PAH HCP CAT Product Owner, Director of Marketing, and will be based in the… 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 ... 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
- Merck & Co. (North Wales, PA)
- …that the requirements for the portfolio of pipeline products are clearly articulated. The Associate Director will report directly to the US Marketing Leader for ... work across the enterprise with colleagues in US Payer Marketing, Global Commercial, Clinical Development, Data & Analytics and Outcomes Research to support the… more
- Merck & Co. (Lower Gwynedd, PA)
- …Us: The Discovery, Preclinical and Translational Medicine Operations (DPTM) is seeking an Associate Director to lead the Molecular lab within the Late ... IT platforms, and science to accelerate vaccines and enable late-stage clinical trials through the generation of timely, high-quality regulated bioanalytical data.… more
- Merck & Co. (North Wales, PA)
- …enrollment and retention efforts to achieve study milestonesUpon request from Global Clinical Trial Operations (GCTO),Recommends study sites and identifies ... Job DescriptionRole SummaryThe Oncology Regional Medical Scientific Director ( Associate RMSD) is a credentialed (ie, PhD, PharmD, DNP, MD) therapeutic and… more
- Takeda Pharmaceuticals (Trenton, NJ)
- …to the best of my knowledge. **Job Description** **Objectives:** As part of the Global Evidence and Outcomes (GEO) team, this position is focused on documenting the ... innovative therapies across the oncology portfolio through: + Analysis of unmet clinical need and potential therapeutic preferences + Development of Clinical … more
- Merck (Trenton, NJ)
- …and Pharmacometrics -** **Immune/Oncology** **(QP2-IO)** team in the role of Associate Director QP2-IO team is part of the Global Clinical Development ... of drug development and effective communication skills. As a subject matter expert, the Associate Director within the QP2-IO Group will work closely with teams… more
- J&J Family of Companies (Spring House, PA)
- Johnson & Johnson is currently seeking an Associate Director , Clinical Development to join our Interventional Oncology team in North America (Spring House or ... unique routes of administration for investigational cancer therapies. The Associate Director , Clinical Development will...and day to day management of one or more global clinical studies, in compliance with department… more
- Merck (West Point, PA)
- **Job Description** The Global Clinical Supply organization is accountable for managing the 'end-to-end' integrated clinical supply chain across the full ... company Research Laboratories portfolio of clinical trials. Global Clinical Supply is accountable for the planning, sourcing, labeling, packaging and… more
- Bristol Myers Squibb (Princeton, NJ)
- …to the Senior Director , Executive and Strategic Communications, the Associate Director , Global Technical Services Communications, is responsible ... executing strategic communication initiatives that support Bristol Myers Squibb's Global Technical Services operations. This role involves crafting high-quality… 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 ... obtain labeling approval by Labeling Senior Management Cross-functional team ( Global Labeling Oversight Committee - GLOC) driving cross-functional collaboration and… more
- Bristol Myers Squibb (Princeton, NJ)
- …work and in their personal lives. Read more: careers.bms.com/working-with-us . **Title:** Associate Director , Program Management, Global Operations (Inline ... cell therapies enabling global regulatory approval and launches. The ** Associate Director , Program Management** plays an important role in organizing,… more
- Takeda Pharmaceuticals (Trenton, NJ)
- …and direct the execution of diversity and inclusion strategy and tactics for global clinical trial programs. + Accountable for the co-creation and implementation ... and technologies that will ensure delivery of diverse participant populations in clinical trials representative of populations anticipated to be treated with the… more
- Bristol Myers Squibb (Princeton, NJ)
- …report results to relevant stakeholders + Create actionable monitoring capabilities for global HCC and anti-bribery compliance monitoring for BMS entities and third ... associated with outsourcing to third parties globally + General understanding of Global HCC laws, regulations, and industry codes; working knowledge of sales,… more
- Merck (Upper Gwynedd, PA)
- …the way we approach serious diseases. The Director will report to an Associate Vice President in the Oncology Clinical Research Group. Under the guidance of ... **Job Description** Our company is a global health care leader with a diversified portfolio...medicines span all phases of clinical development (pre- clinical to post-licensure). The Director will manage… more
