- Daiichi Sankyo, Inc. (Bernards, NJ)
- …well as, develop and effectively manage annual operating plan and budget for the Oncology Medical Strategy Group. Support the US Medical Affairs ... and immune disorders. Responsibilities- Serve as the face of Daiichi Sankyo US Medical Affairs to external stakeholders. Oversee a Medical Affairs oncology… more
- Genmab (Plainsboro, NJ)
- …best, 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 ...Director , US Medical Affairs Solid Tumors Strategy Lead. S/he...Use this knowledge to inform and adapt to the US medical strategy as needed.Develop… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …the company's growth, thereby accomplishing corporate goals.Responsibilities:Develop and implement US regulatory strategy for assigned project(s). Strategize and ... 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 ... technology. With more than 100 years of scientific expertise and a presence in more than 20 countries, Daiichi Sankyo and its 16,000 employees around the world draw upon a rich legacy of innovation and a robust pipeline of promising new medicines to help… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …to the Sr Director , Group Leader, GPM&L or the Executive Director , US Head GPM&L. ResponsibilitiesProject Responsibilities: Independently manage or lead ... to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class...strategy development on Global Project Teams (GPT) for drug… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …PMs assigned to alliance assets for operational matters. Responsibilities:Develop and implement US regulatory strategy for assigned project. Lead and prepare FDA ... to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class...minutes to capture the full discussion for archiving.Serves as US RA strategy SME and coordinates, mentors/instructs,… 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)
- …pharmaceutical therapies to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class science and ... supports oversight and management of integrations solution design, implementation strategy and requirements gathering, and technical feasibility and delivery. The… more
- Genmab (Plainsboro, NJ)
- …leader will be primarily responsible for the development of global (and US ) regulatory strategies (depending on the assigned project/projects) to advance Genmab's ... will provide strategic input and ensure operational execution of global (and US ) submission activities. The individual will be responsible to interface directly with… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …aligned therapeutic / franchise area(s). Relationships Reports to the Executive/Senior Director of Value Communication and Contracting Strategy . Interacts ... Strategy & Portfolio Innovation, PCOR, Brands, Health Economics, Medical Affairs, Account Executives, Analytics, and Global Pricing to develop 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 ... position serves as the Global Regulatory Affairs (GRA) Labeling Strategy expert to the Global Product Team (GPT) as...position drives/leads the development and maintenance of the CCDS, US and EU labeling, and manages the review of… 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 ... position serves as the Global Regulatory Affairs (GRA) Labeling Strategy expert to the Global Product Team (GPT) as...position drives/leads the development and maintenance of the CCDS, US and EU labeling, and manages the review of… more
- Genmab (Plainsboro, NJ)
- …for Genmab's first asset in hematology, EPKINLY. This critical role will report to the Director of Key Customer Strategy and be expected to work closely within ... authentic is essential to fulfilling our purpose.The RoleThe Associate Director , Key Accounts will shape, implement, and execute Key...the US Marketing Team, with EPKINLY cross-functional teams and EPKINLY… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- … serves as a visible PED champion and subject matter expert within the US organization to execute PED strategy initiatives, which ultimately drive a ... of standards and best practices for PED throughout the US organization. Relationships The Director -Patient Centered Outcomes... US affiliate role focused on executing on US PED strategy which encompasses innovative research… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …can work from Plainsboro, NJ facility or remotely form anywhere in the United States . Development of People Supervisory Ensure that reporting personnel have ... About the Department The Clinical, Medical and Regulatory (CMR) department at Novo Nordisk...development, CMR is involved. The one thing that keeps us all marching to the same beat is our… 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 ... and implementing regulatory strategies with the FDA to providing medical education and collecting data to support efficacy and...development, CMR is involved. The one thing that keeps us all marching to the same beat is our… more
- Tris Pharma (Monmouth Junction, NJ)
- …(COEs), Patient Advocacy Groups and Health Care Providers (HCPs) to inform medical strategy ; Conducts regular KOL and emerging customer assessments ensuring ... team success.We have an immediate opening for a Head, Medical Science Liaisons (MSLs) / Director , ...strategies; Works closely with Account Management to develop the Medical Value Strategy and executionEstablishes strategic relationships… 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 ... and implementing regulatory strategies with the FDA to providing medical education and collecting data to support efficacy and...development, CMR is involved. The one thing that keeps us all marching to the same beat is our… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …to make a difference? The Position Reporting to the head of Clinical, medical , Regulatory (CMR) Business Operations, the Associate Director (AD) is responsible ... About the Department The Clinical, Medical and Regulatory (CMR) department at Novo Nordisk...development, CMR is involved. The one thing that keeps us all marching to the same beat is our… more
- Tris Pharma (Monmouth Junction, NJ)
- …Medical , Regulatory review processDemonstrated experience in driving marketing strategy and market development program initiativesProven track record of ... Inc. (www.trispharma.com) is a leading privately-owned biopharmaceutical company in the US with a focus on development and commercialization of innovative medicines… more
