- Merck & Co. (North Wales, PA)
- Job DescriptionRole Summary:The Global Senior Director Medical Affairs (GDMA) Immunology/Pipeline & Biomarkers will be responsible for driving execution of ... medical affairs experience (eg, Regional Director Medical Affairs ) with proven...or SLE or SSc Vitiligo and understanding of the US market)Strong prioritization and decision-making skillsAbility to effectively collaborate… more
- Lundbeck (Chicago, IL)
- …candidates anywhere in the Greater United StatesSUMMARY:The Sr. Dir. Medical Affairs Future Product Portfolio will secure US medical insights for ... especially Digital & Data Analytics function, to accelerate needed infrastructure within US Medical Affairs . We seek a senior, strategic and highly adaptable… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …Board meetings for a Therapeutic Area in certain instances, at the discretion of Executive Director of Medical Affairs . Assists the Senior Medical ... development, CMR is involved. The one thing that keeps us all marching to the same beat is our...portfolio. Relationships This position reports directly to the Executive Director , Medical Affairs and will… more
- Novo Nordisk Inc. (Chicago, IL)
- …of TA priorities and business needs. Relationships This position may report into the Field Director , Medical Affairs (or in smaller TA's directly into the TA ... SD works closely with the TA Leadership Team and Medical Director team to identify and execute...for scientific resources, communications, and training initiatives for the medical affairs team Serve on Clinical Trial… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …Supervise designated personnel. Relationships Report to the Director /Associate Director /Lead Regulatory Scientist/Sr. Manager Regulatory Affairs . Develop and ... 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
- Merck & Co. (North Wales, PA)
- Job DescriptionReports to the Director /Senior Director in the Office of Promotion and Advertising Review (OPAR)The Associate Director is responsible for the ... review and approval of all US promotional materials and serving as the promotional regulatory...as the promotional regulatory expert with marketing, legal, and medical teams to ensure that promotional practices are consistent… more
- Daiichi Sankyo, Inc. (Basking Ridge, 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. (Basking Ridge, 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. (Basking Ridge, 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. (Basking Ridge, NJ)
- …pharmaceutical therapies to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class science and ... trial protocol development and reviews (clinical trial protocols and medical device protocols)ICF reviews to ensure adequate disclosure for collection,… more
- Merck & Co. (North Wales, PA)
- Job DescriptionRole Summary: The Oncology Regional Medical Scientific Director (RMSD) is a credentialed (ie, PhD, PharmD, DNP, MD) therapeutic and disease expert ... of diversityConsistent adherence to field and corporate policies and Global Medical Scientific Affairs (GMSA) strategy, including field standard operating… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionThe Associate Director , Global Marketing will join the New Assets Brand Strategy team and help build the future of our Company's Oncology. This role ... campaign concept development, media planning, content & assets development, medical /legal reviews & approvals, regional execution and budgeting. Launch Excellence… more
- Merck & Co. (North Wales, PA)
- …is a member of several cross-functional teams, including the Promotional Review Team (PRT), and the US and Global Medical Affairs Teams. In PRT, the MCRP is ... with physicians to answer MIRs.-Proactively engage with leaders and participate in US and Global Medical Affairs Teams to ensure that sufficient medical … more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …pharmaceutical therapies to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class science and ... across all major regions, incl. direct reports for the US , EU and China, and indirect accountability for JP...This role will also work with the Global Regulatory Affairs Leadership Team (GRA-LT) to define DS' priorities, strategy… 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)
- …sales, medical /CMR, legal, compliance, and regulatory. Other internal relationships include Public Affairs , Government Affairs & US Corp Giving & Social ... independently in order to accomplish objectives. Relationships Reports to the Director , Patient Support Programs Rare Disease. Key internal relationships include… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …Internal relationships include working with Headquarters, NA CMR including Clinical Trial Management, Medical Affairs , Regulatory Affairs and other NNI skill ... 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)
- …Inc. (www.trispharma.com) is a leading privately-owned biopharmaceutical company in the US with a focus on development and commercialization of innovative medicines ... addressing unmet patient needs. We have more than 150 US and International patents (including applications) and have marketed...opening in our Monmouth Junction, NJ facility for a Director , Drug Safety. The Director , Drug Safety… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …Market Access and Public Affairs , and internal stakeholders from Marketing, Medical Affairs , HEOR, Finance, Commercial, Field Sales, Government Pricing, and ... role is based in Plainsboro, NJ. The Position The Director Market Access Channel Strategy is part of a...and long-term business objectives Ensures close collaboration with MAPA, Medical Affairs , HEOR, Marketing, Finance, and Field… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …stakeholders Interacts internally with Strategic Pricing & Contracting, Finance, Brands, Medical Affairs , HEOR, Commercial Pipeline, Field Sales, Account ... Value Communications, Innovation, Strategic Pricing & Contracting, Marketing, Health Economics, Medical Affairs , Account Executives, Market Access Insights, and… more
