- 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)
- …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
- 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
- Genmab (Plainsboro, NJ)
- …and/or as trial responsible statistician with responsibilities as described below. The Associate Director contributes to clinical development strategies and ... and authentic is essential to fulfilling our purpose.The RoleThe Associate Director acts as a statistical expert...Director acts as a statistical expert supporting the clinical development of compounds as compound and/or indication lead… more
- Merck & Co. (North Wales, PA)
- …that drive IT delivery, including 21-CFR-Part-11, Annex 11, Good Laboratory and Clinical practices, Computer Systems Validation, and other global regulatory ... event reporting and signal detection.-Maintain PV knowledge: Maintain up-to-date knowledge of global PV regulations and guidelines and ensure that the company's PV… 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
- Takeda Pharmaceuticals (Trenton, NJ)
- …bring life-changing therapies to patients worldwide. Join Takeda as an Associate Director , Global Patient Safety Clinical Operations in Cambridge, MA, ... the Pharmacovigilance Operations team, you will report to the Director , PV Clinical Operations and will be...processing to optimize evaluation of safety data stemming from clinical trials + Represent Pharmacovigilance Operations on Global… more
- J&J Family of Companies (Spring House, PA)
- …therapies to patients with immune-mediated diseases. Position Overview: The focus of the Associate Director Clinical Scientist is to support various ... depending on the therapeutic area and trial-specific requirements. The Associate Director Clinical Scientist is...communication skills. + The ability to work in a global matrix organization with cross-functional teams is required. +… more
- Merck (Upper Gwynedd, PA)
- **Job Description** ** Associate Director , Global Oncology Commercial Pipeline Analytics, HHDDA** Our Human Health Digital Data and Analytics (HHDDA) ... data, and analytics to measure our organizational impact. The Associate Director , Global Oncology Commercial...global marketing, operations, finance & enterprise strategy, and clinical & discovery to inform executive decision making and… 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
- Novo Nordisk (Plainsboro, NJ)
- …across multiple functional areas. Relationships You will report to the Senior Director - Global Regulatory Portfolio Lead. Essential Functions + Serve ... 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
- Bristol Myers Squibb (Princeton, NJ)
- …to the Senior Director , GPS Executive and Strategic Communications, the Associate Director , Global Supply Chain Communications and External Affairs, ... and executing strategic communication initiatives that support Bristol Myers Squibb's global supply chain operations and external affairs. This role involves… more
- Bristol Myers Squibb (Princeton, NJ)
- …development and implementation of technical solutions for integrating, analyzing and reporting clinical data. Associate Director drives the development and ... implementation of innovative strategies and technologies for clinical trial programming. Associate Director develop collaborative relationships and work… more
- Merck (Trenton, NJ)
- **Job Description** **Job Description:** The Regional Medical Scientific Associate Director is a credentialed (ie, PhD, PharmD, DNP, MD) therapeutic and disease ... Research, Scientific Congress Support, and Scientific Insights. Regional Medical Scientific Associate Director 's liaise between the scientific community and the… more
- Sumitomo Pharma (Trenton, NJ)
- …position of ** Associate Director , Regulatory Affairs** . The Associate Director is part of the Global Regulatory Affairs (GRA) team based in the US. ... Sumitomo Pharma Co., Ltd. is a global pharmaceutical company based in Japan with key...colleagues, fostering collaboration, and idea sharing + Reviews nonclinical, clinical and CMC documentation (eg nonclinical study reports, … more
- Takeda Pharmaceuticals (Trenton, NJ)
- …company that will inspire you and empower you to shine? Join us as an Associate Director , Data Configuration Engineer in our Cambridge, MA office. At Takeda, we ... and transformation templates for reuse for study level configuration tasks. The Associate Director Data Configuration Engineer (DCE) oversees a team that… more
- System One (King Of Prussia, PA)
- …meets industry and regulatory requirements for clinical trial coding. The Associate Medical Coding Director manages and oversees staff, strategic partners, ... Title: Associate Medical Coding Director Full Time...technology that supports efficient dictionary management processes and with Global Patient Safety and Clinical Development for… more
- Takeda Pharmaceuticals (Trenton, NJ)
- …innovation-driven company to inspire you and empower you to shine? Join us as an Associate Director , GCP Compliance based remotely reporting to the Director , ... research organization, including 6 or more years in compliance or clinical study management required. + Global /international experience required, including… more
- Merck (North Wales, PA)
- …& Division organization of our company. ** ** **Position Description/Summary:** The GPAM Associate Director , Project Manager, is a core member of Early Drug ... Description:** The drug development Project Manager is part of Global Project and Alliance Management (GPAM) which sits in...& Development pipeline and realize its full potential. The Associate Director is expected to provide project… more
- J&J Family of Companies (Horsham, PA)
- …Care Systems Inc. (Strategic Customer Group, SCG) is recruiting for an Associate Director /Product Director , Precision Medicine, Market Access Marketing ... and in-line precision medicine enabled assets. The newly created position of Associate Director /Product Director , Precision Medicine, Market Access Marketing… more
