- Signet Health (Taos County, NM)
- …Taos, NMVista Taos Renewal Center is currently seeking a New Mexico licensed Full-Time Clinical Affairs Director position in Taos, NM.This position delivers ... of convictions for violence-related charges) Minimum two (2) year experience','directApply':true,'datePosted':'2024-03-29T04:00:00.000Z','title':' Clinical Affairs Director - Full-Time','occupationalCategory':'Social… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …Clinical Trial Strategy Team in collaboration with Clinical Operations point, Clinical Director , and Field Medical Affairs point to identify ... Area in certain instances, at the discretion of Executive Director of Medical Affairs . Assists the Senior...for select clinical trials, in collaboration with Clinical Director and Clinical Operations… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …research areas centered around rare diseases and immune disorders.Summary The Senior Director , Global Oncology Medical Affairs is responsible for developing the ... the assigned compound and will report into the Global Oncology Medical Affairs Franchise Head.Responsibilities-Responsible for the development of the Global Medical … more
- Lundbeck (Chicago, IL)
- …to candidates anywhere in the Greater United StatesSUMMARY:The Sr. Dir. Medical Affairs Future Product Portfolio will secure US medical insights for assessment of ... global Lundbeck BD opportunities and pipeline clinical development. Furthermore, the Sr Med Dir will build...Analytics function, to accelerate needed infrastructure within US Medical Affairs . We seek a senior, strategic and highly adaptable… more
- 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 ... and skills: A minimum of 5 years regional medical affairs experience (eg, Regional Director Medical ...to medical affairs strategiesExperience in country/region medical affairs or clinical development (in IBD or… more
- Merck & Co. (North Wales, PA)
- Job DescriptionThe Director , Regulatory Affairs Liaison, is responsible for development and implementation of global regulatory strategy for their assigned ... Development Teams and regulatory single point-of-contact for products within Global Regulatory Affairs and Clinical Safety (GRACS) and external to GRACS.Develops… more
- Merck & Co. (North Wales, PA)
- …knowledge and editorial skills to contribute to medical education and clinical decision support for healthcare professionals, while also providing high quality ... viewed by more than 1 billion users each year.A minimum of 5 years clinical experience and demonstrated writing skills are mandatory. Current clinical activity… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …research areas centered around rare diseases and immune disorders.Summary The Senior Director , Global Oncology Medical Affairs is responsible for developing the ... the assigned compound and will report into the Global Oncology Medical Affairs Franchise Head.Responsibilities- Responsible for the development of the Global Medical… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …in other DSI governance process (DRF, G-PAD, GROC, GRSC etc.) Interfaces with clinical & pre- clinical groups, Regulatory CM&C and other appropriate group within ... the company as needed.ResponsibilitiesManages, directs, and drives the strategy for all Regulatory activities associated with the registration and support of new and approved drug products.Seeks and incorporate regional and functional RA strategy into a global… 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 ... support for anticipated promotional messages and claims (aligned with marketing strategy) in clinical trial design and product labeling as it relates to the use of… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …other research areas centered around rare diseases and immune disorders. SummaryThe Director , Global Oncology Medical Affairs , Evidence Generation role is ... with Global Health Economics Outcomes Research partner.- As a member of Global Medical Affairs Team (GMAT, or Joint Medical Affairs Team for Alliance compounds)… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …other research areas centered around rare diseases and immune disorders.SummaryThe Senior Director , Global Oncology Medical Affairs , Evidence Generation role is ... Evidence Plans (IEP) with the Alliance Partner.- As a member of Global Medical Affairs Team (GMAT, or Joint Medical Affairs Team for Alliance compounds) and… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …areas centered around rare diseases and immune disorders. Summary The Associate Director , GMA Oncology, Scientific Engagement is responsible for the execution of ... activities in support of Global Medical Affairs Scientific Engagement strategies and plan for the Solid Tumor or Hematology therapeutic area (TA), under the guidance… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …those involving 3rd party development. This position partners with GRLs and Clinical Safety Pharmacovigilance (CSPV) leads in the maintenance of Company Core Data ... industry experience required4 or More Years of direct regulatory affairs experience, including US labeling experience requiredExperience with ex-US labeling… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …of a CDx study/IVDR performance evaluation study integration of an assay into clinical testing (before testing) and once data is ready for CDx submission (after ... to external diagnostic business partners specifically:Use of CTA/CDx within clinical trialsDevice protocols and SAPsDevice non-significant/significant risk determinations (both… more
- Eisai, Inc (Nutley, NJ)
- …is your profile, we want to hear from you. Job Summary The Medical Director will provide medical leadership for medical affairs strategy, planning and supportive ... therapeutic area. Under the direction of the Senior Medical Director , this role will be responsible for working with...strategic development, planning, implementation and oversight of Phase IV clinical trial programs within the Medical Affairs … more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …in creation of developmental and regulatory strategy in collaboration with Regulatory Affairs ; Drafts clinical development plans, protocol profiles and sections ... program in a specific indication, ie, multiple multinational phase II/III clinical trials; Reviews regulatory documents from cross functional, holistic perspective;… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …in the assigned therapeutic area. Relationships Reports to the Executive Director - Clinical Research & Development. Internal relationships include working ... with Headquarters, NA CMR including Clinical Trial Management, Medical Affairs , Regulatory Affairs and other NNI skill areas. External relationships include… more
- Merck & Co. (Rahway, NJ)
- …Executive Director , as a senior member of the Global Regulatory Affairs and Clinical Safety: Chemistry, Manufacturing and Controls Organization (GRACS CMC), ... expanding your career.The Chemistry, Manufacturing & Controls (CMC) Pre-approval Pharm Executive Director is accountable for managing a team of CMC professionals and… more
- Novo Nordisk Inc. (Chicago, IL)
- …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 head). ... ready to make a difference? The Position The Scientific Director (SD) functions as a subject matter expert to...scientific resources, communications, and training initiatives for the medical affairs team Serve on Clinical Trial Strategy… more
