• Novo Nordisk Inc. (Plainsboro, NJ)
    …Serve on Local Labeling Committee (LLC) and provide medical input to Regulatory Affairs Physical Requirements 30% overnight travel required; Qualifications MD ... About the Department The Clinical, Medical and Regulatory (CMR) department at Novo Nordisk is one...expert for our products and related data within a Therapeutic Area (Diabetes-GLP-1, Diabetes-Insulins, Cardiorenal Diseases, Obesity, NASH, Rare… more
    HireLifeScience (06/22/24)
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  • Novo Nordisk Inc. (Plainsboro, NJ)
    …teams, including sales, marketing, medical affairs , Centers of Excellence (COEs), regulatory affairs , and other relevant NNI departments to ensure alignment ... to experiment with us? The Position The Consumer Strategist Manager will be a critical driver in shaping an...role will be in the support of the diabetes therapeutic area, specifically the upcoming launch. Relationships Reports to… more
    HireLifeScience (05/15/24)
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  • Senior Manager , Regulatory

    Takeda Pharmaceuticals (Trenton, NJ)
    …to bring life-changing therapies to patients worldwide. Join Takeda as a Senior Manager , Regulatory Affairs Project Management and Strategic Planning where ... therapies to patients. By focusing R&D efforts on four therapeutic areas and other targeted investments, we push the...through proactive engagements with cross functional team members, Global Regulatory Affairs TAU colleagues and Global … more
    Takeda Pharmaceuticals (06/22/24)
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  • Associate Director - Regulatory

    Novo Nordisk (Princeton, NJ)
    …Are you ready to make a difference? The Position The Associate Director, Regulatory Affairs - Advertising & Promotion will provide strategic regulatory ... Relationships Develop and maintain positive rapport and working relationships with Regulatory Affairs , Legal, Commercial, and other cross-functional stakeholders… more
    Novo Nordisk (05/09/24)
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  • Medical Director-Medical Affairs - Obesity

    Novo Nordisk (Plainsboro, NJ)
    …+ Serve on Local Labeling Committee (LLC) and provide medical input to Regulatory Affairs Physical Requirements 30% overnight travel required; Qualifications + ... About the Department The Clinical, Medical and Regulatory (CMR) department at Novo Nordisk is one...expert for our products and related data within a Therapeutic Area (Diabetes-GLP-1, Diabetes-Insulins, Cardiorenal Diseases, Obesity, NASH, Rare… more
    Novo Nordisk (06/22/24)
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  • Senior Manager , Global Regulatory

    Takeda Pharmaceuticals (Trenton, NJ)
    …and delivers transformative therapies to patients. By focusing R&D efforts on four therapeutic areas and other targeted investments, we push the boundaries of what ... negotiations with Health Authorities. + Ensures labeling content conform to regulatory requirements. Management of Local Exceptions and LOC Interactions + Manages… more
    Takeda Pharmaceuticals (06/18/24)
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  • Publications Manager

    Kelly Services (Plainsboro, NJ)
    …from Medical Affairs , Clinical Data Science & Evidence, legal, regulatory affairs , global publication team, and commercial publications colleagues from ... Kelly is hiring for a **Publications Manager ** position with one of our clients in...and execution of publication plan(s) across assigned therapies and therapeutic areas. + This position tracks (database entry), updates,… more
    Kelly Services (05/31/24)
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  • Sr. Director, Senior Safety Officer- Johnson…

    J&J Family of Companies (Titusville, NJ)
    …continuous improvement and developing trusting partnerships internally (eg R&D, Quality, Regulatory , Commercial, Legal, Medical Affairs ) and externally (eg ... of the Safety Management Teams (SMTs) and / or manager or Medical Safety Officers (MSOs) who lead SMTs,...is preferred. Additional education or experience in clinical, medical affairs , regulatory , epidemiology or biostatistics preferred +… more
    J&J Family of Companies (06/15/24)
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  • Project Manager A

    University of Pennsylvania (Philadelphia, PA)
    …health and wellness programs and resources, and much more. Posted Job Title Project Manager A Job Profile Title Manager Research Project A Job Description ... Summary The Project Manager will coordinate multiple efforts. This includes clinical coordinating...Monitoring participant health and safety throughout the study. + Regulatory Compliance and Study Planning and Preparation: Assisting in… more
    University of Pennsylvania (04/24/24)
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  • Innovation Manager - Digital Health…

    Nestle (Philadelphia, PA)
    Manager will work closely with NHSc brand, product, R&D, marketing, legal, regulatory , IT, and medical affairs teams locally and globally to define and ... NJ Office. **Position Summary:** We are seeking an experienced Strategic Programs Manager to lead select projects in digital health across Nestle Health Science… more
    Nestle (06/19/24)
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  • Medical Science Liaison, GU Oncology - Urology- NJ…

    J&J Family of Companies (Trenton, NJ)
    …GU Oncology - Urology- NJ & DE - 2406193107W **Description** Janssen Scientific Affairs , LLC, a member of Johnson & Johnson's Family of Companies, is recruiting ... staying abreast of current scientific and treatment landscape trends in the relevant therapeutic areas and providing research support for the company as well as… more
    J&J Family of Companies (06/19/24)
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  • Director, Worldwide Medical Oncology, Professional…

    Bristol Myers Squibb (Princeton, NJ)
    …MS with general knowledge of pharmaceutical operations, ie, advocacy, medical affairs , clinical development, regulatory , commercialization, + Understanding of ... professional societies, including initiatives and programs in alignment with specific therapeutic area strategic imperatives. + Should be familiar with the disease… more
    Bristol Myers Squibb (06/21/24)
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  • Associate Principal Scientist, Oncology…

    Merck (Trenton, NJ)
    …Evidence, Global Discovery, Preclinical and Translational Medicine, Global Medical and Scientific Affairs , and Global Regulatory Affairs and Clinical Safety ... and maintain an awareness of key data and insights within assigned therapeutic area(s)/product(s) to convey our Research & Development Division data effectively and… more
    Merck (06/22/24)
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  • Clinical Research Coordinator B/C (Hybrid…

    University of Pennsylvania (Philadelphia, PA)
    …and various sponsors. This position will report directly to the Program Manager and work directly with Physician Investigators ("PI") on clinical research performed. ... subject recruitment, detailed data entry, subject visits, and follow-up and regulatory documentation. The successful candidate will comply with all policies relating… more
    University of Pennsylvania (06/14/24)
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  • Clinical Research Coordinator C (Department…

    University of Pennsylvania (Philadelphia, PA)
    …recruitment, detailed data entry, subject visits and follow-up and regulatory documentation. Position contingent upon funding. Job Description Responsibilities + ... monitoring, internal and external auditing, and study close-out visits. Interface with regulatory authorities, Sponsors and cooperative groups as directed by the … more
    University of Pennsylvania (06/21/24)
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  • Clinical Research Coordinator B (Department…

    University of Pennsylvania (Philadelphia, PA)
    …The Clinical Research Coordinator B (CRC-B) will report directly to a Project Manager within the 2-PREVENT Breast Cancer Translational Center of Excellence (TCE) and ... will focus on coordinating non- therapeutic longitudinal and observational protocols. The CRC-B will have...monitoring visits and audits, 5) Assist the TCE Project Manager , Program Director, and/or PI with preparing materials for… more
    University of Pennsylvania (04/19/24)
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