- Organon & Co. (Plymouth Meeting, PA)
- …Director in Organon Regulatory Chemistry, Manufacturing and Controls (CMC), the Associate Principal Scientist is responsible for developing and ... with global regulations and guidances, and Organon procedures. The Associate Principal Scientist will lead...products and be accountable for the delivery of all regulatory milestones for assigned products through the product lifecycle.?… more
- Organon & Co. (Plymouth Meeting, PA)
- …**The Position?** Reporting to the Director in Organon Regulatory CMC,?the Associate Principal Scientist is responsible for?developing and?implementing ... products in accordance with global regulations and?guidance, and?Organon procedures.? The Associate Principal Scientist will lead the?preparation and… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionJOB DESCRIPTION SUMMARY Primary activities include but are not limited to: The Associate Principal Scientist is a DVM and/or PhD whose primary ... clinical laboratory and field studies that will support the regulatory approval of new companion animal and livestock products....studies, and occasionally Good Laboratory Practice (GLP) studies. The Associate Principal Scientist is the… more
- Merck & Co. (Rahway, NJ)
- …therapeutic areas and routes of administration, including inhalation, implantation, and injection.The Associate Principal Scientist will lead the definition ... the clinical instruction(s) and commercial market approval(s) of combination products. Principal ResponsibilitiesLead, set direction, align with key stakeholders, and… more
- Merck & Co. (Rahway, NJ)
- …process validation, second generation process development and authoring of regulatory submissions.-We are seeking a strategic and technical leader with ... Provide technical oversight of cell culture process development, process characterization and regulatory filing activities to ensure a smooth and clear path to… more
- Merck & Co. (Rahway, NJ)
- …art scientific methodologies and tools to enable the discovery, development, regulatory approval, manufacturing, and marketing of medical drugs and vaccines for ... the span of which range from individual clinical trials to world-wide regulatory application submissions and post marketing support.The incumbent is responsible for… more
- Merck & Co. (North Wales, PA)
- …span of which range from individual clinical trials to world-wide regulatory application submissions and post marketing support.-Design and maintain statistical ... and systems and database expertise;US and/or worldwide drug or vaccine regulatory application submission experience at the leadership level including the development… more
- Merck & Co. (Boston, MA)
- Job DescriptionThe Senior Director (Sr. Principal Scientist ) has primary responsibility for the planning and directing clinical research activities involving new ... including development strategy, study design, initiation, execution, monitoring, analysis, regulatory reporting, and publication.Specifically, the Senior Director May Be… more
- Merck (Rahway, NJ)
- …Description** **JOB DESCRIPTION SUMMARY** _Primary activities include but are not limited to:_ The Associate Principal Scientist is a DVM and/or PhD whose ... clinical laboratory and field studies that will support the regulatory approval of new companion animal and livestock products....studies, and occasionally Good Laboratory Practice (GLP) studies. The Associate Principal Scientist is the… more
- IQVIA (Indianapolis, IN)
- We are seeking a **Senior Scientist /** ** Associate Principal Scientist , Ligand Binding Assays** to join IQVIA Laboratories in **Indianapolis, IN** . We ... join us as we transform and accelerate research and development. As a Senior Scientist / Associate Principal Scientist , you will provide technical… more
- Merck (Rahway, NJ)
- …areas and routes of administration, including inhalation, implantation, and injection. The Associate Principal Scientist will lead the definition and ... clinical instruction(s) and commercial market approval(s) of combination products. ** Principal Responsibilities** + Lead, set direction, align with key stakeholders,… more
- Merck (West Point, PA)
- …Description** We are seeking a motivated and experienced Translational PET Imaging Scientist to lead the transition of novel PET radiotracers from late preclinical ... on clinical implementation of novel PET tracers in oncology studies, guide regulatory submissions, and act as the PET imaging expert within multidisciplinary project… more
- Amgen (South San Francisco, CA)
- …Join us and transform the lives of patients while transforming your career. ** Principal Scientist - Clinical Pharmacology, Modeling & Simulation** **What you ... Modeling & Simulation Department at Amgen is seeking a Principal Scientist . In this vital role, you...of Clinical Pharmacology and Modeling & Simulation experience **Or** Associate 's degree and 10 years of Clinical Pharmacology and… more
- Merck (Rahway, NJ)
- …investigations, process validation, second generation process development and authoring of regulatory submissions. We are seeking a strategic and technical leader ... Provide technical oversight of cell culture process development, process characterization and regulatory filing activities to ensure a smooth and clear path to… more
- Merck (Rahway, NJ)
- …art scientific methodologies and tools to enable the discovery, development, regulatory approval, manufacturing, and marketing of medical drugs and vaccines for ... the span of which range from individual clinical trials to world-wide regulatory application submissions and post marketing support. The incumbent is responsible for… more
- Merck (North Wales, PA)
- …the span of which range from individual clinical trials to world-wide regulatory application submissions and post marketing support. + Design and maintain ... systems and database expertise; + US and/or worldwide drug or vaccine regulatory application submission experience at the leadership level including the development… more
- Amgen (Washington, DC)
- …us and transform the lives of patients while transforming your career. **Senior Principal Scientist - Global Diagnostic Development Lead** **What you will do** ... assay to marketed Diagnostic to support the clinical development strategy for regulatory approval and commercialization. As such, the Dx group works closely with… more
- Regions Bank (Atlanta, GA)
- …into the careers section of the system. **Job Description:** At Regions, the Principal Data Scientist is a visionary and hands-on practitioner that supports ... unless required by law. Such information will be stored in accordance with regulatory requirements and in conjunction with Regions' Retention Schedule for a minimum… more
- Walmart (Bentonville, AR)
- …service operations and technology solutions for Finance, People, and the Associate Digital Experience. **About People.AI Team** The People.AI team is responsible ... intelligent experience within a chatbot or business application to enhance associate experience and productivity. You will design and build an intelligent… more
- University of Colorado (Aurora, CO)
- **Open Rank - Assistant, Associate , Professor. Lead Scientist in Psychiatric Neuromodulation Research.** **Description** **University of Colorado Anschutz** ... value-added recruitment advertising agency (https://www.jobelephant.com/) Open Rank - Assistant, Associate , Professor. Lead Scientist in Psychiatric Neuromodulation… more
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