- 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
- 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)
- …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)
- … to post-licensure). With a focus on late-stage development, the Senior Director will manage the entire cycle of clinical development, including study ... with key opinion leaders. Specifically, the Senior Director May Be Responsible For: Evaluating pre- clinical ...clinical findings from studies to support decisions regarding safety and efficacy as well as new drug applications,… 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)
- …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
- 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
- Novo Nordisk Inc. (Plainsboro, NJ)
- …capabilities through strategic vendor partnerships. Relationship This job reports to the Senior Director of the GxP Compliance & Technical Operations. This ... a strategic leader for the role of GxP Patient Safety , Compliance & Vendor Oversight within our Clinical... Safety , Compliance & Vendor Oversight within our Clinical , Medical & Regulatory (CMR) organization. This position combines… 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
- Novo Nordisk Inc. (Plainsboro, NJ)
- About the Department The Clinical , Medical and Regulatory (CMR) department at Novo Nordisk is one of the most diverse and collaborative groups within the ... case handling issues, and process improvements related to patient safety . Relationship Reports to the Head of NNI Patient...Digital Enablement). This role will provide direct guidance to senior managers and managers involved in case triage, case… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …training delivery in a highly regulated environment. Relationship This job reports to the Senior Director of the GxP Compliance & Technical Operations or the GxP ... About the Department The Clinical , Medical and Regulatory (CMR) department at Novo...Compliance, Patient Safety , Vendor Oversight Director . This job will… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …within the pharmaceutical or biotechnology industry. Relationship This job reports to the Senior Director of the GxP Compliance & Technical Operations or the ... About the Department The Clinical , Medical and Regulatory (CMR) department at Novo Nordisk... Director , GxP Compliance, Patient Safety , & Vendor Oversight.… more
- Jobleads-US (Rahway, NJ)
- …principles to enhance patient safety and product usability. The Senior Director will champion enterprise-wide HF strategy, foster cross-functional ... Overview Job Description The 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… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …technologies to elevate employee performance and growth. Relationship This job reports to the Senior Director of the GxP Compliance & Technical Operations or the ... About the Department The Clinical , Medical and Regulatory (CMR) department at Novo...GxP Compliance, Patient Safety , Vendor Oversight Director . This job will… more
- Integra LifeSciences (Princeton, NJ)
- …training programs for US-based healthcare customers. Under the guidance of the Director of Professional Education this will include planning, execution and budget ... external stakeholders to include Marketing, Legal, Compliance, Field Sales Leadership, Clinical Specialists, Medical Affairs, and HCP Faculty. **ESSENTIAL DUTIES AND… 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
- Regeneron Pharmaceuticals (Warren, NJ)
- …projects through early and late phase development. The Director reports to the Senior Director Clinical Sciences and collaborates closely with Medical ... The Director Clinical Sciences, Hematology, leads in...Regulatory Authorities) + Performs and mentors direct reports in clinical /medical data review, including safety monitoring and… more
- Bristol Myers Squibb (Madison, 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
