- Merck & Co. (Rahway, NJ)
- …Atherosclerosis & Metabolism medicines span all phases of clinical development (pre- clinical to post-licensure). The Senior Director will manage the ... monitoring, analysis, regulatory reporting, and publication.Specifically, the Senior Director May Be Responsible For: Evaluating pre- clinical and… more
- Merck & Co. (Rahway, NJ)
- …Oncology medicines. Our Oncology medicines span all phases of clinical development (pre- clinical to post-licensure). The Senior Director will manage the ... report to an Associate Vice President in the Oncology Clinical Research Group. Under the guidance of...compounds. In executing these duties, the Senior Director may: Supervise the activities of Clinical … more
- Merck & Co. (Rahway, NJ)
- …involving investigational compounds in Immunology. With a focus on late-stage development, the Senior Clinical Director will manage the entire cycle of ... monitoring, analysis, regulatory filing, and publication.Specifically, The Senior Director May Be Responsible For:Evaluating pre- clinical and translational… more
- Merck & Co. (Rahway, NJ)
- Job Description Role Summary: The Global Senior Director Medical Affairs (GDMA) is a subject matter expert in their area of responsibility (eg, defined tumor, ... Serves as the medical representative within Product Development sub-teams (including Clinical , V&I, Commercial, Publications, and Label), leveraging the GMSA vision… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionThe Senior Director of Human Factors (HF) will provide visionary leadership and strategic direction for the HF function within our company. This ... of HF principles to enhance patient safety and product usability. The Senior Director will champion enterprise-wide HF strategy, foster cross-functional… more
- Merck & Co. (Rahway, NJ)
- …and execute design verification strategies that successfully supports the clinical instruction(s) and commercial market approval(s) of combination products.Principal ... strategies for assigned drug-device combination product program(s) for successful clinical introduction(s) and commercial market(s) approval(s).Define design input(s)/ output(s)… more
- Merck & Co. (Rahway, NJ)
- …execution globally across Global Regulatory Affairs CMC (Global Regulatory Affairs & Clinical Safety), Research and Development (R&D), Manufacturing, and Global ... and dedicated colleagues while developing and expanding your career.The Executive Director , Chemistry, Manufacturing & Controls ( CMC) , Pre-approval Pharm will… more
- Merck & Co. (Rahway, NJ)
- …represent the brand performance and agenda, priorities, and performance with senior level stakeholders for Small Molecule products across Global Pharmaceutical ... Gain alignment and endorsement for supply chain strategic elements through senior stakeholder management and appropriate executive governance forums. Develop and… more
- Merck & Co. (Rahway, NJ)
- Job Description Role Summary The Associate Director of Procurement for Capital Projects will be responsible for overseeing and managing procurement activities for a ... ensuring compliance with company policies and processes. - Reporting to the Director of Capital Procurement Project Execution within the Global Capital Procurement… more
- Merck & Co. (Rahway, NJ)
- …applicants for a Principal Scientist position available at its Rahway, New Jersey research facility. The Principal Scientist is a senior scientific role tasked ... Job DescriptionThe Biologics Analytical Research & Development department of our company ...with working closely with the group Director to define group strategy and to lead a… more
- Formation Bio (New York, NY)
- …pharma companies, research organizations, and biotechs to develop programs past clinical proof of concept and beyond, ultimately helping to bring new medicines ... than the industry can progress because of the high cost and time of clinical trials. Recognizing that this development bottleneck may ultimately limit the number of… more
- Formation Bio (New York, NY)
- …pharma companies, research organizations, and biotechs to develop programs past clinical proof of concept and beyond, ultimately helping to bring new medicines ... than the industry can progress because of the high cost and time of clinical trials. Recognizing that this development bottleneck may ultimately limit the number of… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …areas centered around rare diseases and immune disorders. Job Summary: The GCO Senior Director of Study Optimization has accountability for the oversight, ... with regulatory guidance (eg, FDA, EMA, NIH) on diversity and inclusion in clinical research . Establish best practices, training and resources for internal teams… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- … areas centered around rare diseases and immune disorders. Job Summary: The Sr. Director , Clinical Safety MD, will lead the development and implementation of ... primarily focused on providing novel therapies in oncology, as well as other research areas centered around rare diseases and immune disorders. Under the Group's… more
- Eisai, Inc (Nutley, NJ)
- …mgmt. activities. #LI-CCEisai Salary Transparency Language:The base salary range for the Senior Director , Clinical Quality Assurance - Remote-Based is ... in neurology and oncology, with a strong emphasis on research and development. Our history includes the development of...your profile, we want to hear from you. The Clinical Quality Assurance Professional (QAP) position is responsible for… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- … Director US Medical Affairs (USMA) Oncology, under the direction of the Senior Director , USMA Oncology (US Medical Affairs team lead for compound), is ... Sankyo is primarily focused on providing novel therapies in oncology, as well as other research areas centered around rare diseases and immune disorders. SummaryThe… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …leader for assigned compound under the supervision and leadership of the Executive Director of Medical Research and Strategy, US Oncology Medical Affairs ... focused on providing novel therapies in oncology, as well as other research areas centered around rare diseases and immune disorders. SummaryUS Medical Affairs… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …focused on providing novel therapies in oncology, as well as other research areas centered around rare diseases and immune disorders. SummaryMedical Affairs leader ... as a member of the various cross-functional forums including, Publications Planning, Clinical and Safety sub-teams, and Global Product Team to inform clinical… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …utilization of innovative translational strategies across the continuum of research /preclinical and clinical stages preferred.- Experience/knowledge in companion ... providing novel therapies in oncology, as well as other research areas centered around rare diseases and immune disorders....goals and enumerate key scientific questions that will drive clinical development decision-making. In doing so, he or she… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …focused on providing novel therapies in oncology, as well as other research areas centered around rare diseases and immune disorders. Summary:The primary ... drug registration or for any project with CDPs containing multiple registrational clinical trials and are extensively exploring the predictive nature of potential… more
