• Merck & Co. (North Wales, PA)
    Job Description Position Description: Associate Director , Regulatory Affairs Liaison- Vaccines and Infectious Disease The Regulatory Affairs ... the Vaccine and Infectious Disease (VID) therapeutic area as part of a regulatory team. They will have excellent communication and collaboration skills and will work… more
    HireLifeScience (06/06/24)
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  • Novo Nordisk Inc. (Plainsboro, NJ)
    …Relationships Report to the Director / Associate Director /Lead Regulatory Scientist/Sr. Manager Regulatory Affairs . Develop and maintain positive ... Position Manage and oversee all assigned projects/products/processes. Assist the Director / Associate Director in assuring Novo...rapport and working relationships with other personnel in Regulatory Affairs , CMR, and other local and… more
    HireLifeScience (06/05/24)
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  • Novo Nordisk Inc. (Plainsboro, NJ)
    …lives for a living. Are you ready to make a difference? The Position The Associate Director , Medical Affairs Omnichannel Engagement, role is to support the ... About the Department The Clinical, Medical and Regulatory (CMR) department at Novo Nordisk is one...the medical affairs omnichannel engagement strategy. The Associate Director - MOE will work with one… more
    HireLifeScience (06/06/24)
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  • Merck & Co. (Rahway, NJ)
    …and solutions to the world.Looking for someone with a growth mindset. The Director , Regulatory Affairs Liaison is responsible for:Developing regulatory ... Job DescriptionOur Regulatory Affairs team bring new medical...activities include, but are not limited to:Reports to Executive Director or Associate Vice President, Therapeutic Area… more
    HireLifeScience (05/22/24)
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  • Daiichi Sankyo, Inc. (Basking Ridge, NJ)
    …as other research areas centered around rare diseases and immune disorders.SummaryThe Associate Director (AD) is responsible for overseeing all activities ... and is also an integral member of the Medical Affairs Team. This position plays a key role in...data and promotional content within the assigned therapeutic area- Regulatory milestones, actions and guidance relevant to medical review… more
    HireLifeScience (06/04/24)
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  • Daiichi Sankyo, Inc. (Basking Ridge, NJ)
    …Years pharmaceutical industry experience required4 or More Years of direct regulatory affairs experience, including US labeling experienceExperience with ex-US ... This position serves as the GRA labeling expert to the Global Regulatory Team (GRT) and independently provides strategic and operational leadership on product… more
    HireLifeScience (06/03/24)
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  • Daiichi Sankyo, Inc. (Basking Ridge, NJ)
    …research areas centered around rare diseases and immune disorders. Summary The Senior Director , Head Global PV Quality (DSI/DSE) reports to the Global Head RDPVQA, ... and oversees multiple levels of direct reports (Directors, Associate Directors, Managers, contractors as applicable) across the Global PV Quality teams located in… more
    HireLifeScience (06/01/24)
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  • Novo Nordisk Inc. (Plainsboro, NJ)
    …clinical trials is required Demonstrates technical expertise within Clinical Development, Medical Affairs , and Regulatory Affairs (CMR), staying up-to-date ... About the Department The Clinical Development, Medical and Regulatory (CMR) department at Novo Nordisk is one of the most diverse and collaborative groups within the… more
    HireLifeScience (04/26/24)
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  • Novo Nordisk Inc. (Plainsboro, NJ)
    …focusing on optimizing patient care and support. Relationships Reports to the Director of PSP Analytics and Ops Excellence. Key internal relationships include ... and Reimbursement, Finance, IT, etc. Other internal relationships include Public Affairs and CMR. External relationships include relations with external consultants,… more
    HireLifeScience (05/11/24)
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  • Daiichi Sankyo, Inc. (Basking Ridge, NJ)
    …statistical results and provide input on reporting (CSR) to support Medical Affairs and HEOR/HTA strategies: Plan, set-up and execute additional statistical analyses ... Statistical deliverables. Contribute, with limited supervision, to documents submitted to Regulatory or Pricing Authorities. May participate as subject matter expert… more
    HireLifeScience (05/17/24)
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  • Merck & Co. (North Wales, PA)
    …studiesWork closely with a cross-functional group of experts in commercialization, regulatory affairs , statistics, and manufacturing to manage clinical ... cycle of clinical development, including: study design, placement, monitoring, analysis, regulatory reporting, and publication.-Specifically, the Director may be… more
    HireLifeScience (05/30/24)
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  • Insmed Incorporated (Bridgewater, NJ)
    …in Biopharma™, Best Workplaces in New York™, and Best Workplaces for Millennials™ lists.OverviewThe Associate Director , HCP Marketing will be a key member of the ... our culture. This position will report to the Senior Director , HCP and Payer Lead. This position does not...and media agencyWork closely with cross-functional partners including Legal, Regulatory , Compliance, and Medical Affairs , to align… more
    HireLifeScience (04/04/24)
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  • Merck & Co. (Rahway, NJ)
    …Work closely with a cross-functional group of experts in commercialization, regulatory affairs , statistics, and manufacturing to manage clinical development ... regulatory filing, and publication. Specifically, The Senior Clinical Director May Be Responsible For: Evaluating pre-clinical and translational work for… more
    HireLifeScience (05/25/24)
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  • Concorde Career Colleges, Inc. (Jacksonville, FL)
    Overview Join Our Mission: Shape the Future of Healthcare as a Director of Nursing! Are you a compassionate and dedicated nurse looking to make a profound impact on ... experienced nurses like you are the driving force behind this transformation. As the Director of Nursing, you will have the opportunity to share your wealth of… more
    JobGet (06/06/24)
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  • Associate Director

    Taiho Oncology (Princeton, NJ)
    Associate Director , Regulatory Affairs Strategy Pleasanton, CA, USA * Princeton, NJ, USA Req #374 Thursday, May 30, 2024 Looking for a chance to make a ... and/or development regulatory activities under the direction of Regulatory Affairs management. The incumbent plans, directs and executes the regulatory more
    Taiho Oncology (05/31/24)
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  • Associate Director

    Teva Pharmaceuticals (West Chester, PA)
    Associate Director , Regulatory Affairs - Remote OR West Chester, PA Date: May 15, 2024 Location: West Chester, United States, Pennsylvania, 19380 ... new people to make a difference with. **How you'll spend your day** As the Associate Director , Regulatory Affairs you will be responsible for acting as… more
    Teva Pharmaceuticals (05/16/24)
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  • Associate Director

    BD (Becton, Dickinson and Company) (Covington, GA)
    **Job Description Summary** As Associate Director , Regulatory Affairs , you will be responsible for managing a team that develops and executes the ... updates, risks and regulation or guidance changes to Corporate Quality and Regulatory Affairs . International Regulatory Affairs and Senior Leadership.… more
    BD (Becton, Dickinson and Company) (04/09/24)
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  • Associate Director

    Novo Nordisk (Princeton, NJ)
    …changing lives for a living. Are you ready to make a difference? The Position The Associate Director , Regulatory Affairs - Advertising & Promotion will ... strong and positive working relationship with OPDP reviewers. Report to Senior Director , Regulatory Affairs - Advertising & Promotion. Essential Functions +… more
    Novo Nordisk (05/09/24)
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  • Associate Director

    Merck (North Wales, PA)
    **Job Description** **Position Description:** ** Associate Director , Regulatory Affairs Liaison- Vaccines and Infectious Disease** The Regulatory ... the Vaccine and Infectious Disease (VID) therapeutic area as part of a regulatory team. They will have excellent communication and collaboration skills and will work… more
    Merck (06/06/24)
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  • Associate Director

    Regeneron Pharmaceuticals (Basking Ridge, NJ)
    The Associate Director Regulatory Affairs will provide leadership on global regulatory activities for the assigned products. Responsibility will ... mainly focus on Clinical Regulatory filings and provide regulatory leadership on the project teams in this area. We are a hands-on culture so responsibilities… more
    Regeneron Pharmaceuticals (05/11/24)
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