- 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 Strategy Lead. S/he will provide medical affairs leadership for assigned asset(s)/indications and… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …a living. Are you ready to make a difference? The Position The Associate Director , Regulatory Affairs - Advertising & Promotion will provide strategic regulatory ... About the Department The Clinical, Medical and Regulatory (CMR) department at Novo Nordisk...positive working relationship with OPDP reviewers. Report to Senior Director , Regulatory Affairs - Advertising & Promotion.… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …and adoption/uptake of standards and best practices for PED throughout the US organization. Relationships The Director -Patient Centered Outcomes Research reports ... development, CMR is involved. The one thing that keeps us all marching to the same beat is our...Medical and Regulatory (CMR), Market Access and Public Affairs (MAPA), as well as collaborating where appropriate with… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …representatives. Interacts internally with team representatives from PCOR, Finance, Brands, Medical Affairs , HEOR, Commercial Pipeline, Field Sales, Account ... Value Communications, Strategy & Portfolio Innovation, PCOR, Brands, Health Economics, Medical Affairs , Account Executives, Analytics, and Global Pricing to… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …sales, medical /CMR, legal, compliance, and regulatory. Other internal relationships include Public Affairs , Government Affairs & US Corp Giving & Social ... and personal development. Are you ready to maximize your potential with us ? The Position Responsible for developing patient solution strategies that maximize access… more
- Genmab (Plainsboro, NJ)
- …Security Operations TeamBusiness leaders (eg, VP Medical Affairs , VP Regulatory Affairs , GM Genmab US , IT Lead in Japan)Peers within IT&D, such as ... will include stakeholders in the business domains Field Operations, Medical & Regulatory Affairs and US...and IT&D leaders, with a main focus in the United States .IT&D Partner: Acts as security partner… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …with cross-functional teams, including members of the CDSE team, clinical development, medical affairs , regulatory, and commercial, to facilitate the integration ... development, CMR is involved. The one thing that keeps us all marching to the same beat is our...of stakeholders across CDSE and more broadly within Clinical, Medical and Regulatory, Market Access and Public Affairs… 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 ... strongly preferred Expert understanding of the pharmaceutical industry including marketing, medical , access, public affairs , compliance, legal and regulatory as… 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...development, CMR is involved. The one thing that keeps us all marching to the same beat is our… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …reports to a Director Level Team Member within Scientific Communications (SC), Medical Affairs . The Manager-Publications is expected to develop and utilize a ... development, CMR is involved. The one thing that keeps us all marching to the same beat is our...with local and global publication stakeholders, including colleagues from Medical Affairs , Clinical Data Science & Evidence,… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- … Team, PCOR (Pricing, Contracting, Operations and Reimbursement), Marketing, Commercial Sales, Medical Affairs , Legal & Compliance and Human Resources. External ... Care Pharmacy Providers, National and Regional Federal Organizations such as Veterans Affairs and associated medical centers, Department of Defense and… 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 ... team success.We have an immediate opening for a Head, Medical Science Liaisons (MSLs) / Director , ...Adverse Events (AEs) and Product Quality Complaints (PQCs)Collaborates with VP/ Medical Affairs to ascertain and secure resources… 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 ... 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
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …pharmaceutical industry experience required4 or More Years of direct regulatory affairs experience, including US labeling experience requiredExperience with ex- ... 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 ... development plans. The individual will direct, coordinate and implement the preparation of US regulatory submissions and provide US regulatory support across all… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …will be responsible for bringing the issue and potential solutions to the Head of US Regulatory Affairs in conjunction with the assigned US RA strategist ... to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class...and transparent ways of working across the Alliance within US regulatory affairs and will work closely… 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 ... development plans. The individual will direct, coordinate and implement the preparation of US regulatory submissions and provide US regulatory support across all… 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 ... into the Oncology drug development preferred.Ability to interpret and understand US regulations governing the pharmaceutical industry; general global knowledge of… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …pharmaceutical industry experience required4 or More Years of direct regulatory affairs experience, including CCDS and US /EU labeling experience ... pharmaceutical industry experience required4 or More Years of direct regulatory affairs experience, including US labeling experienceExperience with ex- US… more
