- Novo Nordisk Inc. (Plainsboro, NJ)
- …lives for a living. Are you ready to make a difference? The Position The Senior Director of CMR Knowledge & Technical Advancement (KTA) Department will serve to ... About the Department The Clinical , Medical and Regulatory (CMR) department...strategy they will provide valuable support and consultation to Senior Leaders in the Line of Business. In this… 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 ... Are you ready to make a difference? The Position Senior , Clinical Informatics leads the functions in...individual will serve as a subject matter expect on clinical and medical informatics software and system… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …HQ. Key internal relationships include Project Managers, Clinical Directors, Medical Affairs directors, HEOR Directors, Market Access director , Marking ... About the Department The Clinical , Medical and Regulatory (CMR) department...ready to make a difference? The Position The Strategy Director is a senior individual contributor role,… more
- Merck & Co. (Rahway, NJ)
- …manufacturing to manage clinical development projects; and Assist the Senior /Executive Director /AVP in ensuring that appropriate corporate personnel are ... medicines span all phases of clinical development (pre- clinical to post-licensure). The Director will manage...percent of the time to manage future or ongoing clinical research projects. -Provide scientific and medical … more
- Merck & Co. (Rahway, NJ)
- Job DescriptionRole Summary: The Global Senior Director Medical Affairs (Sr GDMA), Hematology is responsible for driving the development and execution of the ... expertiseMinimum of 6 years Hematology and Oncology experienceAt least 3 years regional medical affairs experience (eg, Regional Director of Medical Affairs)… 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 ... least 10 of those most recent years working as an employee in clinical , medical and/or regulatory in the pharmaceutical industry (Pharma/Biotech/CRO) A minimum… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …centered around rare diseases and immune disorders. SummaryThe Senior Director sits within Global Oncology Clinical Development, an organization dedicated ... clinical trials. Serves as a primary source of medical accountability and oversight for one or more ...medical accountability and oversight for one or more clinical trials Matrix management responsibilities across the internal and… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …submission documents under guidance of higher level. Reviews and oversee completion of clinical trial protocols. Provides medical and/or scientific direction to ... pharmaceutical therapies to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class science and… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …research areas centered around rare diseases and immune disorders. SummaryReporting to the Senior Director , I&A, the Associate Director , Global Oncology ... global guidance provided to regions across DS. The Associate Director serves as a strategic partner to senior...this role including Marketing, Supply Chain, Finance, Market Access, Medical Affairs and Clinical Development.- Partner with… more
- Merck & Co. (North Wales, PA)
- Job DescriptionRole Summary:The primary role of the US Executive Director , Field Medical Affairs, Health Systems Oncology (EDFMA-HSO) is the leadership, ... experience in the pharmaceutical industryDemonstrated learning agility and experience managing medical teamsAbility to effectively engage senior management to… more
