• Merck & Co. (Rahway, NJ)
    Job DescriptionPosition Description: Senior Scientist (Early Clinical Scientist ) The Early Clinical Scientist /ECS coordinates the design, planning and ... issue identification and resolution skills Knowledge of GCP, ICH guidelines and regulatory requirements Preferred Experience and Skills:- Global Phase I subject… more
    HireLifeScience (04/30/24)
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  • Merck & Co. (North Wales, PA)
    …art scientific methodologies and tools to enable the discovery, development, regulatory approval, manufacturing, and marketing of medical drugs and vaccines for ... the benefit of patients and global human health. Responsibilities :Develops, coordinates, and provides biostatistical support for related drug/vaccine projects under… more
    HireLifeScience (05/02/24)
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  • Merck & Co. (Rahway, NJ)
    …with talented and dedicated colleagues while developing and expanding your career.The Senior Director (Sr. Principal Scientist ) has primary responsibility for ... of clinical development, including study design, placement, monitoring, analysis, regulatory reporting, and publication.Specifically, The Senior Director May… more
    HireLifeScience (04/27/24)
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  • Merck & Co. (Rahway, NJ)
    Job DescriptionPosition Description: Senior Scientist - Cell-based Biological Characterization, Cell-Based Sciences AR&D We are seeking a highly motivated ... Senior Scientist to join our functional characterization...partner organizations (eg, early discovery, process development, analytical development, regulatory and quality control organizations).We are looking for candidates,… more
    HireLifeScience (04/25/24)
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  • Merck & Co. (Rahway, NJ)
    …products and processes are developed in accordance with applicable regulatory , quality, company, and customer requirements.-This position will lead cross-functional ... integration of the device development activities with the clinical, regulatory , formulation, commercial and other key company functions.Represent Device Development… more
    HireLifeScience (05/02/24)
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  • Merck & Co. (Rahway, NJ)
    …This position will focus on oncology products.Under the direction of a HEDS Senior Director, the Principal Scientist provides strategic development and use of ... art scientific methodologies and tools to enable the discovery, development, regulatory approval, manufacturing, and marketing of medical drugs and vaccines for… more
    HireLifeScience (04/30/24)
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  • Merck & Co. (Rahway, NJ)
    Job DescriptionPosition Description: Principal Scientist , Upstream Bio Process Development BPR&D within our Company's Research Laboratories is on a mission to ... and engage with the scientific community to influence the field.As a Principal Scientist you will have the opportunity to influence the future direction of our… more
    HireLifeScience (04/25/24)
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  • Merck & Co. (Rahway, NJ)
    Job DescriptionOur company is a global health care leader with a diversified portfolio of prescription medicines, vaccines and animal health products. Today, we are ... an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated… more
    HireLifeScience (04/23/24)
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  • Daiichi Sankyo, Inc. (Basking Ridge, NJ)
    …medicines to help people. Under the Group's 2025 Vision to become a " Global Pharma Innovator with Competitive Advantage in Oncology," Daiichi Sankyo is primarily ... The Associate Director, RACMC Portfolio Products, will be responsible for regulatory CMC (Chemistry, Manufacturing, and Controls) activities of the portfolio small… more
    HireLifeScience (03/01/24)
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  • Daiichi Sankyo, Inc. (Basking Ridge, NJ)
    …medicines to help people. Under the Group's 2025 Vision to become a " Global Pharma Innovator with Competitive Advantage in Oncology," Daiichi Sankyo is primarily ... complexity in design and geographic scope). Prepares clinical section of regulatory document. Collaborates as team member with AROs/CROs. Drafts development plans,… more
    HireLifeScience (03/01/24)
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  • Merck & Co. (North Wales, PA)
    …talented and dedicated colleagues while developing and expanding your career.The Senior Clinical Director (Sr. Principal Scientist ) has primary responsibility ... of clinical development, including: study design, placement, monitoring, analysis, regulatory reporting, and publication.- Specifically, the Senior Director… more
    HireLifeScience (04/30/24)
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  • Merck & Co. (Rahway, NJ)
    …DescriptionOur Clinical Research and Pharmacovigilance team push the boundaries of global healthcare through research and innovation. Through clinical trials and ... existing and pipeline products to produce safe, effective, innovative medicine.The Global Clinical Data Standards Vocabulary Specialist, Associate Director, is a… more
    HireLifeScience (04/19/24)
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  • Senior Regulatory Scientist

    L'Oreal USA (Clark, NJ)
    …(https://careers.loreal.com/en\_US/content/Home) / Job Search (https://careers.loreal.com/en\_US/jobs/SearchJobs) / 178051 Senior Regulatory Scientist II, ... Research & Innovation Full - Time 15-Apr-2024 Position Title: Senior Regulatory Scientist II, ...Review raw materials and formulations to ensure compliance with global regulatory standards + Provide advice to… more
    L'Oreal USA (04/16/24)
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  • Senior Scientist - Corporate…

    Balchem (Montvale, NJ)
    Senior Scientist - Corporate Regulatory Affairs Department: Legal/ Regulatory Location: Montvale, NJ Start Your Application ... reviews. + Define the scope and quality of information required to meet global regulatory objectives, including product authorizations and claims of product… more
    Balchem (03/27/24)
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  • Global Pharmacovigilance (PV) Senior

    Amgen (Washington, DC)
    …10 million patients worldwide. It's time for a career you can be proud of. ** Global Pharmacovigilance (PV) Senior Scientist , Obesity - US Remote** **Live** ... Let's change the world. In this vital role the Global PV Senior Scientist will...Author Safety Assessment Reports and other safety documents and regulatory responses in collaboration with the GSO + Search… more
    Amgen (05/02/24)
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  • Senior Clinical Scientist I, Skin…

    L'Oreal USA (Clark, NJ)
    …as Product Safety, Regulatory Affairs and Claims Legal teams. As a Senior Scientist in our Skin Clinical and Instrumental Evaluation Intelligence Team, your ... check out our website (https://careers.loreal.com/en\_US/content/ResearchInnovations?3\_4\_3=128) We are seeking a Senior Scientist I with an innovative mindset… more
    L'Oreal USA (04/23/24)
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  • Senior Formulation Scientist

    Catalent Pharma Solutions (Greendale, IN)
    …as Quality by Design (QbD), Design of Experiment (DOE), and compliance with all regulatory guidelines. Senior Scientist will be responsible for defining ... and manufacturing challenges. Reporting to the Director Product Development, the ** Senior Scientist ** will provide and utilize technical direction and… more
    Catalent Pharma Solutions (03/16/24)
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  • Senior Principal Scientist

    Amgen (Washington, DC)
    …to excel in a highly collaborative, matrixed team environment + Knowledge of global regulatory guidance and extensive experience with writing scientific reports, ... patients worldwide. It's time for a career you can be proud of. ** Senior Principal Scientist , Pharmacokinetics & Drug Metabolism** **Live** **What you will… more
    Amgen (04/19/24)
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  • Senior Clinical Innovation Research…

    L'Oreal USA (Clark, NJ)
    …/ Job Search (https://careers.loreal.com/en\_US/jobs/SearchJobs) / 178524 Senior Clinical Innovation Research Scientist ... NJ, New Jersey Research & Innovation Full - Time 24-Apr-2024 Position Title: Senior Clinical Innovation Research Scientist I, Advanced Research Location : Clark,… more
    L'Oreal USA (04/25/24)
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  • Senior Scientist , Early Clinical…

    Merck (West Point, PA)
    **Job Description** **Position Description:** ** Senior Scientist (Early Clinical Scientist )** The Early Clinical Scientist /ECS coordinates the design, ... guidelines and regulatory requirements * **Preferred Experience and Skills:** + Global Phase I subject and patient trials, safety reporting, and regulatory more
    Merck (04/30/24)
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