- Genmab (Plainsboro, NJ)
- …and authentic is essential to fulfilling our purpose.The Role The Director of US Medical Affairs Solid Tumors Strategy will report to the Senior ... Director , US Medical Affairs Solid Tumors Strategy ...Director , US Medical Affairs Solid Tumors Strategy Lead. S/he will...will lead the development and execution of the US Medical Affairs strategy that is… more
- Tris Pharma (Monmouth Junction, NJ)
- …leadership of a small MSL team. Collaborating closely with, and reporting directly to, VP/ Medical Affairs in developing medical strategic and tactical plans ... and report Adverse Events (AEs) and Product Quality Complaints (PQCs)Collaborates with VP/ Medical Affairs to ascertain and secure resources and support needed… more
- Tris Pharma (Monmouth Junction, NJ)
- …and compliant communication between marketing and other cross-functional teams (ie, Medical Affairs , Sales, Regulatory Affairs , Operations, etc.)Collaborates ... Medical , Regulatory review processDemonstrated experience in driving marketing strategy and market development program initiativesProven track record of… more
- Genmab (Plainsboro, NJ)
- …team, in particular security architects and Genmab Security Operations TeamBusiness leaders (eg, VP Medical Affairs , VP Regulatory Affairs , GM Genmab US, IT ... focus of this role will include stakeholders in the business domains Field Operations, Medical & Regulatory Affairs and US and Japan Market and Commercial Teams… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …role will closely partner with Field Sales, Market Access, Commercial Excellence, Medical Affairs , Strategic Partnerships and Engagement, Customer Experience and ... About the Department The Strategy & Rare Disease (STARS) organization drives the...preferred Expert understanding of the pharmaceutical industry including marketing, medical , access, public affairs , compliance, legal and… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …implementing/facilitating, maintaining technical training programs related to GxP, Clinical, Medical and Regulatory affairs , Patient Safety required A ... About the Department The Clinical, Medical and Regulatory (CMR) department at Novo Nordisk...ready to make a difference? The Position The Senior Director of CMR Knowledge & Technical Advancement (KTA) Department… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …Relationships Member of the Market Access & Public Affairs (MAPA) Channel Strategy Team, reporting to Director , Market Access Medicare Strategy . ... potential? The Position The Senior Manager Market Access Channel Strategy is part of a team responsible for developing...Public Affairs , and internal stakeholders from Marketing, Medical Affairs , HEOR, Finance, Commercial, Field Sales,… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …Board, Patient Marketing, Managed Markets, Trade, Corporate Communications, Legal, Regulatory, Medical Information and Medical Affairs . External ... approval meetings and liaising/coordinating with all agencies involved Work with Associate Director on digital customer engagement strategy for conventions by… more
- Merck & Co. (Rahway, NJ)
- …stakeholder communication tools in collaboration with Commercial, R&D, Outcomes Research, Medical Affairs , Policy, Communications, and with regional and local ... the AVP Global Market Access, Global Pharma, the Executive Director , Global Market Access, Infectious Disease & Ophthalmology will...and Product Development Teams (PDTs), (ex. clinical, OR and medical affairs ), regional and country teams to… more
- Insmed Incorporated (New York, NY)
- …to ensure adequate training, access to educational resources and alignment between Insmed's medical affairs plans and the unmet needs of the patients and ... research and development programs as requested by R&D, Clinical Operations, and Medical Affairs Departments. This may include trial site identification, ongoing… more
- Merck & Co. (Rahway, NJ)
- …Senior/ Executive Director group of experts in commercialization, regulatory affairs , statistics, medical affairs and manufacturing to manage ... applying rigorous scientific and ethical standards.-The Distinguished Scientist (Executive Director ) and Product Development Team (PDT) lead, Oncology Global… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …pharmaceutical therapies to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class science and ... growth, thereby accomplishing corporate goals.Responsibilities:Develop and implement US regulatory strategy for assigned project(s). Strategize and plan for FDA… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …pharmaceutical therapies to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class science and ... growth, thereby accomplishing corporate goals.ResponsibilitiesDevelop and implement US regulatory strategy for assigned project(s).Strategize and plan for FDA meetings… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …pharmaceutical therapies to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class science and ... Qualifications7 or More Years in the pharmaceutical industry4 or More Years in regulatory affairs , NDA, sNDA, BLA filing to FDA Travel Ability to travel up to 30%… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …pharmaceutical therapies to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class science and ... for bringing the issue and potential solutions to the Head of US Regulatory Affairs in conjunction with the assigned US RA strategist on the assets. This role… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …pharmaceutical therapies to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class science and ... disorders. Summary: Responsible for leading and developing global regulatory strategy for assigned development projects. Represents Daiichi Sankyo's regulatory group… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …Clinical Safety and Pharmacovigilance, Regulatory/Risk Management, Quality Assurance, Medical Affairs , Translational Research, Research, Informatics Services, ... 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)
- …rare diseases and immune disorders. SummaryThis position serves as the Global Regulatory Affairs (GRA) Labeling Strategy expert to the Global Product Team (GPT) ... 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)
- …rare diseases and immune disorders. Summary This position serves as the Global Regulatory Affairs (GRA) Labeling Strategy expert to the Global Product Team (GPT) ... 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)
- …pharmaceutical therapies to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class science and ... and external functions including Clinical Development, Research Development, Regulatory Affairs . Facilitate operational meetings with CROs, License Partners, and PV… more
