- Daiichi Sankyo, Inc. (Bernards, NJ)
- …research areas centered around rare diseases and immune disorders. Job Summary: The Sr. Director , Clinical Safety MD, will lead the development and ... regulatory agency or academia, with exposure to drug development, clinical pharmacology, and/or epidemiology.Oncology expertise requiredClinical safety … more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …function as a member of the various cross-functional forums including, Publications Planning, Clinical and Safety sub-teams, US and Global Brand Team, and US ... compound under the supervision and leadership of the Executive Director of Medical Research and Strategy, US Oncology Medical...Product Team to inform clinical development, commercialization, market access, and other cross-functional strategic… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …function as a member of the various cross-functional forums including, Publications Planning, Clinical and Safety sub-teams, and Global Product Team to inform ... model the way and enable the team to act.Provides medical leadership to:- GMA clinical operations teams as part of evidence generation forums and study teams for… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …across all Medical Affairs programs. This role involves deputizing for the Sr. Director , representing the Quality organization at senior levels. The Director ... centered around rare diseases and immune disorders. Job Summary: Reporting to the Sr. Director , Medical Affairs QA, the Director of Medical Affairs QA is… more
- 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 ... clinical findings from studies to support decisions regarding safety and efficacy as well as new drug applications,...compounds. In executing these duties, the Senior Director may: Supervise the activities of Clinical … 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)
- …principles to enhance patient safety and product usability. The Senior Director will champion enterprise-wide HF strategy, foster cross-functional ... Job DescriptionThe Senior Director of Human Factors (HF)...to the HF team and key stakeholders across R&D, clinical , regulatory, marketing, manufacturing, and quality functions.Educate and build… 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)
- …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
- Formation Bio (New York, NY)
- …role, you'll pioneer the development of sophisticated models to predict clinical outcomes-determining drug efficacy, safety profiles, and optimal indications-to ... 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
- 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 (Rahway, NJ)
- …Oncology medicines. Our Oncology medicines span all phases of clinical development (pre- clinical to post-licensure). The Senior Director will manage the ... clinical findings from studies to support decisions regarding safety and efficacy as well as new drug applications,...compounds. In executing these duties, the Senior Director may: Supervise the activities of Clinical … more
- Merck (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
- Otsuka America Pharmaceutical Inc. (Trenton, NJ)
- …lead the clinical development activities in support of domestic and international clinical development initiatives. The Senior Director , GCD works in a ... clinical trials and regulatory filing activities. The Senior Director , GCD is responsible for all...potential for meeting an unmet medical need, establishing early clinical safety and proof of concept, conduct… more
- J&J Family of Companies (Titusville, NJ)
- …profoundly impact health for humanity. Learn more at https://www.jnj.com/. **POSITION SUMMARY:** The Senior Director , Clinical Leader (CL) is responsible for ... supplies unit, data management, medical writing, biostatistics, global medical safety , pharmacogenomics, early clinical development, clinical pharmacology,… more
- Sumitomo Pharma (Trenton, NJ)
- …seeking a dynamic, highly motivated, and experienced individual for the position of Senior Medical Director , Clinical Research (Ophthalmology) to join our ... working with the safety group to ensure adequacy of safety monitoring and reporting + Provide clinical input for and participate in study set up and design… more
- J&J Family of Companies (Titusville, NJ)
- …at https://www.jnj.com/innovative-medicine **POSITION SUMMARY:** The incumbent will serve as a Senior Director , Clinical Leader in Neurodegeneration, ... development plans or program-related issues + Working with global clinical operations, Regulatory, and Global Medical Safety ,...global clinical operations, Regulatory, and Global Medical Safety , leads the clinical team in responding… more
- Bristol Myers Squibb (Princeton, NJ)
- …personal lives. Read more: careers.bms.com/working-with-us . **Position Summary** This ** Senior Director ,** **Immunology & Neuroscience (I&N), Medical Evidence ... organization are executed with speed and rigor. The I&N Senior Director will lead and participate in...ICF, providing medical input during protocol development to ensure clinical relevance, scientific rigor, patient safety , and… more
- RWJBarnabas Health (West Orange, NJ)
- Director of System Clinical Quality PerformanceReq #:0000190918 Category:Quality / Patient Safety Status:Full-Time Shift:Day Facility:RWJBarnabas Health ... and healthcare acquired infection reduction, supporting system operational excellence in clinical quality, patient safety and patient experience performance. The… more
