- Merck & Co. (Rahway, NJ)
- Job DescriptionThe Global Senior Director of Medical Affairs (GDMA) for Melanoma coordinates the development of the Global Scientific and Medical Affairs ... Cycle Management decisions. In addition, the leads the Medical Affairs input into the Value and Evidence Plan (V&I)...asset value proposition, insights from affiliates and regions, and clinical and value evidence gaps. Translate these Goals and… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …areas centered around rare diseases and immune disorders. Job Summary: Reporting to the Sr. Director , Medical Affairs QA, the Director of Medical Affairs ... programs. This role involves deputizing for the Sr. Director , representing the Quality organization at senior ...expertise in the involvement of regulated activities for medical affairs , or clinical development. requiredMust possess a… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionThe Executive Director (ED) for US Medical Affairs (USMA) understands Our Company's enterprise level strategies and leads cross-functionally with ... with Global Clinical Trial Operations (GCTO) and the broader Global Clinical Development (GCD)-Coordinates with Global Medical Scientific Affairs to ensure… more
- Eisai, Inc (Nutley, NJ)
- …If this is your profile, we want to hear from you. The Medical Director will provide medical leadership for medical affairs strategy, planning and supportive ... for assigned therapeutic area. Under the direction of the Senior Medical Director , this role will be...strategic development, planning, implementation and oversight of Phase IV clinical trial programs within the Medical Affairs … more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- … Director US Medical Affairs (USMA) Oncology, under the direction of the Senior Director , USMA Oncology (US Medical Affairs team lead for compound), ... engagement. Responsible for managing budgets and resources for the assigned medical affairs plan activities, in collaboration with Sr. Director .- Leads medical… more
- Merck & Co. (North Wales, PA)
- Job DescriptionThe Executive Director , Scientific Affairs (EDSA) maximizes meaningful bi-directional scientific exchange with the worldwide clinical and ... studies program in partnership with late-stage development teams in Medical Affairs while also supporting early-stage development teams. The role also partners… more
- Insmed Incorporated (San Diego, CA)
- …for Women™, Best Workplaces for Millennials™, and Best Medium Workplaces™ lists.OverviewThe Director , Regulatory Affairs will serve as the regulatory leader on ... teamsCommunicating regulatory strategies and risk assessments to cross-functional teams and senior leadership, as neededCollaborate with Clinical Development, … more
- Merck & Co. (Upper Gwynedd, PA)
- …Oncology medicines. Our Oncology medicines span all phases of clinical development (pre- clinical to post-licensure). The Senior Director will manage the ... compounds. In executing these duties, the Senior Director may: Supervise the activities of Clinical ...regulatory affairs , statistics, and manufacturing to manage clinical development projects; and Assist the Executive Director… more
- Merck & Co. (Boston, MA)
- …Atherosclerosis & Metabolism medicines span all phases of clinical development (pre- clinical to post-licensure). The Senior Director will manage the ... monitoring, analysis, regulatory reporting, and publication.Specifically, the Senior Director May Be Responsible For: Evaluating pre- clinical and… more
- Merck & Co. (Rahway, NJ)
- …with talented and dedicated colleagues while developing and expanding your career.The Senior Clinical Director (Sr. Principal Scientist) has primary ... team. Our Company's Oncology medicines span all phases of clinical development (pre- clinical to post-licensure). The Senior Director will manage the… more
- Merck & Co. (Rahway, NJ)
- …and respiratory medicines. With a focus on late-stage development, the Senior Director will manage the entire cycle of clinical development, including study ... analysis, regulatory reporting, and publication.Specifically, the Senior Director may be responsible for:Evaluating pre- clinical and translational… more
- Merck & Co. (Rahway, NJ)
- … to post-licensure). With a focus on late-stage development, the Senior Director will manage the entire cycle of clinical development, including study ... will interact externally with key opinion leaders. Specifically, the Senior Director May Be Responsible For: Evaluating pre- clinical and translational work… more
- Merck & Co. (Rahway, NJ)
- …Our company's oncology medicines span all phases of clinical development (pre- clinical to post-licensure).The Senior Director will manage the entire ... analysis, regulatory reporting, and publication. Specifically, the Senior Director may be responsible for:Evaluating pre- clinical and translational work… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …drug registration or for any project with CDPs containing multiple registrational clinical trials and are extensively exploring the predictive nature of potential ... activities and deliverables in collaboration with diagnostic partner across all clinical trials within the project, including the timely deployment of CDx… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …Director Global Medical Affairs Oncology (GMA), under the direction of the Senior Director / Director , GMA Oncology (Global Medical Affairs team ... medical education and other scientific exchange activities in alignment with the Senior Director , such as scientific symposium and medical congresses, within… more
- Eisai, Inc (Nutley, NJ)
- …Medical Education and Training colleagues and with the Global & US MALT (Medical Affairs Leadership Team) to develop and maintain all Medical Affairs training ... judgment; b) effectively communicate relevant and fair balanced scientific and clinical information about Eisai's products; seek feedback from MSLs, MSL Management… more
- Eisai, Inc (Nutley, NJ)
- …If this is your profile, we want to hear from you. Associate Director , Medical Education - Oncology, is responsible for the strategic planning and execution ... of relevant medical communications deliverables aligned with the Medical Affairs strategic plan for assigned therapeutic area(s). These deliverables include… more
- Merck & Co. (Rahway, NJ)
- …and reimbursement. The incumbent is expected to work cross-functionally with clinical development, medical affairs , biostatistics, market access, commercial, and ... and promotion of our company's products.Develops a strong matrix relationship with clinical development, medical affairs , market access, commercial, and key… more
- Genmab (NJ)
- …be within Global Regulatory Affairs (GRA) and will report to the Sr. Director , Labeling, Policy and Intelligence. The position may be based in our Princeton, New ... have you join us!The Global Regulatory Labeling, Policy and Intelligence Associate Director will primarily be responsible for leading the development and maintenance… more
- Merck (Rahway, NJ)
- **Job Description** The Global Senior Director of Medical Affairs (GDMA) for Melanoma coordinates the development of the Global Scientific and Medical ... Affairs Plans for their assigned asset(s). Sr. GDMA collaborate...asset value proposition, insights from affiliates and regions, and clinical and value evidence gaps. + Translate these Goals… more
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