• 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
    HireLifeScience (06/22/24)
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  • Eisai, Inc (NJ)
    …difference. If this is your profile, we want to hear from you. The Medical Director , US Medical Affairs provides medical leadership for medical affairs ... provides strategic development, planning, implementation and oversight of Phase IV clinical trial programs within the Medical Affairs department for products… more
    HireLifeScience (05/28/24)
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  • Eisai, Inc (Nutley, NJ)
    …If this is your profile, we want to hear from you.The Associate Director , Strategic Content Development, Global Medical Affairs - Alzheimer's Disease, in ... alignment and collaboration with all stakeholders. Under the direction of the Director , Strategic Scientific Content Development, Global Medical Affairs , this… more
    HireLifeScience (06/08/24)
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  • Merck & Co. (Rahway, NJ)
    …our products is developed and realized. Role Summary: The Executive Director , Scientific Affairs (EDSA) maximizes meaningful bi-directional scientific exchange ... Job DescriptionOur Medical Affairs team advances medical science and patient care...with the worldwide clinical and academic community to positively impact Research and… more
    HireLifeScience (06/29/24)
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  • Eisai, Inc (Nutley, NJ)
    …#IND123 #LI-Remote Eisai Salary Transparency Language:The base salary range for the Director , Real World Evidence, Global Medical Affairs is from ... difference. If this is your profile, we want to hear from you. The Director is responsible for developing RWE strategies for assigned product(s) and execution of RWE… more
    HireLifeScience (06/30/24)
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  • Daiichi Sankyo, Inc. (Basking Ridge, NJ)
    …research areas centered around rare diseases and immune disorders. Job Summary:The Director , Global Medical Affairs (GMA), Gyn Oncology, under the direction ... of the Senior Director , GMA Oncology (Global Medical Affairs team...drives execution for assigned projects in collaboration with GMA Clinical Operations and other cross-functional and regional stakeholders. Provides… more
    HireLifeScience (04/30/24)
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  • Eisai, Inc (Nutley, NJ)
    …Associate Director , Global RWE (Real World Evidence), Global Medical Affairs - Neurology is from :181,000-237,600Under current guidelines, this position is ... this is your profile, we want to hear from you. Summary The Associate Director is responsible for developing RWE strategies for assigned product(s) and execution of… more
    HireLifeScience (06/25/24)
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  • Novo Nordisk Inc. (Plainsboro, NJ)
    …any time throughout the annual performance cycle. Relationships Reports to Executive Director or Vice President Medical Affairs . Has direct supervisory ... About the Department The Clinical , Medical and Regulatory (CMR) department at Novo...support representatives in answering physicians questions Works with Executive Director to define therapeutic area disease and treatment concepts… more
    HireLifeScience (06/01/24)
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  • 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
    HireLifeScience (06/12/24)
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  • Genmab (Princeton, NJ)
    …diverse antibody products in immuno-oncology and beyond. Reporting to the Global Medical Affairs Strategy Lead (MASL) the Director will be responsible for the ... as part of the asset life cycle management. The Director should have a strong background and experience in...departments to coordinate the planning, execution, and management of clinical trial activities across medical affairs functions… more
    JobGet (07/03/24)
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  • Daiichi Sankyo, Inc. (Basking Ridge, NJ)
    …for diagnostics and devices.Provide strategic input on key development documents, clinical protocols, study reports, IBs, INDs, CTAs, IDEs, SRDs, PMAs and ... dossier documents for submissions globally. Ensure high quality collaboration with Clinical Biomarker and Companion Diagnostics team for development of biomarker,… more
    HireLifeScience (06/22/24)
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  • 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
    HireLifeScience (05/22/24)
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  • Genmab (Far Hills, NJ)
    …our expanding US Medical Affairs (USMA) team, Genmab is seeking a Senior Director , USMA Solid Tumor Portfolio. This role will report to the VP/Head of US Medical ... and relevant studies Provides US market input to Global clinical development and Global Medical Affairs programs,...to Global clinical development and Global Medical Affairs programs, staying abreast of the evolving scientific &… more
    JobGet (07/03/24)
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  • Genmab (Princeton, NJ)
    …Science Liaisons, and other internal Genmab employees. The goal of Medical Affairs is to bridge clinical development and commercialization by communicating ... other serious diseases. This position is within IT in support of the Medical Affairs area. This position supports digital products where the end users are Health… more
    JobGet (07/03/24)
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  • Genmab (Princeton, NJ)
    …an experienced and passionate leader to be a part of our Global Regulatory Affairs (GRA) organization. In this role, you will be primarily responsible for the ... Lead the Global Regulatory Team (GRT) and Submission Team(s). Participate in Clinical Trial Teams, as required for the assigned project(s). For approved products,… more
    JobGet (07/03/24)
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  • Careerbuilder-US (Foster City, CA)
    …role is within the LIFE (Liver, Inflammation, Fibrosis and Established Products) Medical Affairs organization and reports to the Executive Director of Global ... Research, Marketing, Global Commercial Product Strategy, Value and Market Access, Clinical Research, Public Affairs , Government Affairs , Contracts/Finance,… more
    JobGet (07/01/24)
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  • Tris Pharma (Monmouth Junction, NJ)
    …in our Monmouth Junction, NJ facility for an experienced MD to serve as Senior Director or Director , Clinical Development. Title and salary commensurate with ... Development, Research and Development (R&D), Quality Assurance (QA), Pharmacovigilance, Medical Affairs , etc.) on strategic and tactical clinical development… more
    HireLifeScience (06/07/24)
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  • Daiichi Sankyo, Inc. (Basking Ridge, NJ)
    …managing the multiple Clinical Science Asset Leaders (CSALs) at the Senior Director level for each respective program. This Clinical Science (CS) Group Lead ... in one or several programs.Partner and collaborate with RD leaders in Clinical Operations, Biostatistics and Data Management, Regulatory Affairs , and other… more
    HireLifeScience (05/16/24)
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  • Daiichi Sankyo, Inc. (Basking Ridge, NJ)
    …and immune disorders. SummaryThis new role is within R&D reporting into Global Clinical Operations (GCO) and the fundamental responsibility is dedicated to GCO. This ... the successful delivery of study diversity plans in adherence with Good Clinical Practices (GCPs), appropriate Standard Operating Procedures (SOPs), Food and Drug… more
    HireLifeScience (06/19/24)
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  • 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
    HireLifeScience (05/09/24)
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