• Daiichi Sankyo, Inc. (Basking Ridge, NJ)
    …research areas centered around rare diseases and immune disorders. Summary The Director , Clinical Safety , will be a product safety lead or part of a ... product safety team, and be responsible for overall ...may function as a key member of the Global Product Team in collaboration with Clinical Development ,… more
    HireLifeScience (05/09/24)
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  • OSI Group (Aurora, IL)
    This role is responsible for directing the activity of the corporate Product Development department in support of organization objectives. This position will ... and building leadership talent and capability within R&D.Lead and oversee the product development team in a dynamic a fast-paced manufacturing… more
    JobGet (05/15/24)
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  • Tris Pharma (Monmouth Junction, NJ)
    …is responsible for planning, directing, coordinating and prioritizing activities of the product safety team and providing oversight of Pharmacovigilance (PV) ... opening in our Monmouth Junction, NJ facility for a Director , Drug Safety . The Director ,...and PV issues Provides input and expertise to aggregate safety reports (ie, development safety more
    HireLifeScience (04/05/24)
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  • Daiichi Sankyo, Inc. (Basking Ridge, NJ)
    safety is diligently considered prior to selecting promising candidates (DP0), allowing product safety leaders (PSLs) and global project teams (GPTs) to enact ... in R&D as early as possible. This led us to create the Translational Patient Safety Senior Director position, which will have unique exposure to Daiichi Sankyo's… more
    HireLifeScience (03/01/24)
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  • Merck & Co. (Rahway, NJ)
    Job Description Position Description: Director , Business Development Responsible for leading and executing business development and commercial activities ... product costs, intellectual property, quality, capital needs, environmental, safety and industrial hygiene, inventory and production plan, compliance and… more
    HireLifeScience (05/09/24)
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  • Merck & Co. (North Wales, PA)
    …help people with cancer across the globe.This individual serves as the: Associate Director , US Oncology Campaign Development Lead (CDL) - OCAR This individual ... process (Promotion Review Team experience).Experience with accelerated approvals, binder development , & safety label updatesVeeva/PromoMats experienceAgency management… more
    HireLifeScience (05/10/24)
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  • Fidelity TalentSource LLC (Boston, MA)
    Job Description: Director , Product Management The RoleThis role will lead product development within one of the Fidelity Center for Applied Technology ... priorities based on business needs and KPIsStrong technical skills and product development process experienceDemonstrated creativity and design-savvy skillsA… more
    JobGet (05/15/24)
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  • Fidelity TalentSource LLC (Merrimack, NH)
    …or a closely related field and six (6) years of experience as a Director , Product Management (or a closely related occupation) implementing and maintaining risk ... or a closely related field and four (4) years of experience as a Director , Product Management (or a closely related occupation) implementing and maintaining risk… more
    JobGet (04/29/24)
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  • Daiichi Sankyo, Inc. (Basking Ridge, NJ)
    …research areas centered around rare diseases and immune disorders.Summary The Senior Director sits within Global Oncology Clinical Development , an organization ... consistent with CDP and aligned to achieve the Target Product Profile (TPP)- Development of clinical sections...May review tables, listings, and figures (TLF) and CSR safety narratives- May lead the development and… more
    HireLifeScience (05/15/24)
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  • Catalent (Manassas, VA)
    …the Associate Director , Regulatory Affairs is to support regulatory strategy for product development and manufacturing activities for the Cell & Gene Therapy ... Associate Director , Regulatory Affairs Position Summary: Catalent is a...a leading partner for the pharmaceutical industry in the development and manufacturing of new treatments for patients worldwide.… more
    HireLifeScience (05/03/24)
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  • Eisai, Inc (NJ)
    …communication/publication components of overall medical operating plan. The Medical Director provides strategic development , planning, implementation and ... profile, we want to hear from you. The Medical Director , US Medical Affairs provides medical leadership for medical...assigned therapeutic area to provide strategic input for the development of product strategies and liaises with… more
    HireLifeScience (04/26/24)
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  • Eisai, Inc (Nutley, NJ)
    …knowledge in assigned therapeutic area to provide strategic input for the development of product strategies and liaise with external stakeholders to ... and oncology, with a strong emphasis on research and development . Our history includes the development of...want to hear from you. Job Summary The Medical Director will provide medical leadership for medical affairs strategy,… more
    HireLifeScience (04/26/24)
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  • Merck & Co. (Rockville, MD)
    …Laboratories divisions and most directly with Global Regulatory Affairs and Clinical Safety (GRACS) to define and implement a prioritized plan for policy that ... to support the company's enterprise policy agenda.Responsibilities of the Director , US Regulatory Policy, will include:Proactively monitoring emerging scientific and… more
    HireLifeScience (05/09/24)
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  • Fidelity TalentSource LLC (Boston, MA)
    …inquires related to the investment methodology underpinning our solutionsSupport further product development efforts related to Retail, Workplace, Institutional ... (5+) plus years of financial services experience, preferably in product management, product development or...weeks). At Fidelity, we value honesty, integrity, and the safety of our associates and customers within a heavily… more
    JobGet (04/29/24)
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  • Fidelity TalentSource LLC (Boston, MA)
    …will require owning the product roadmap, interpreting market needs and working with development and design teams to bring the product to life.Own the ... Job Description:RoleAs a member of the Product Strategy team at Fidelity Digital Assets\u2120, you...weeks). At Fidelity, we value honesty, integrity, and the safety of our associates and customers within a heavily… more
    JobGet (05/03/24)
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  • Merck & Co. (North Wales, PA)
    …and associated documentation. Provides expertise as worldwide regulatory representative to Product Development Teams and regulatory single point-of-contact for ... by regulatory agencies for multiple indications simultaneously.Provides expert advice to Product Development Teams and subsidiaries on regulatory issues as… more
    HireLifeScience (04/19/24)
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  • Catalent (Philadelphia, PA)
    Position: Director QualityLocation: Philadelphia, PAPosition Summary: The Quality function is to build, monitor, and sustain a robust and effective quality system ... and Australian agencies and other international and/or local health authorities.The Director of Quality is responsible for providing leadership and Quality… more
    HireLifeScience (04/09/24)
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  • Legend Biotech USA, Inc. (Raritan, NJ)
    …Conduct risk assessments to prioritize investigations based on potential impact on product quality, patient safety , and regulatory compliance. Address recurring ... the treatment of multiple myeloma. Legend Biotech is seeking an Associate Director for Operations Compliance and Investigations Managementas part of the Technical… more
    HireLifeScience (04/19/24)
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  • Fidelity TalentSource LLC (Westlake, TX)
    … (TDD), automation, and DevSecOps. Designs User Experiences (UXs) and leads new product development . Draws on in-depth knowledge of the business or function ... field and six (6) years of experience as a Director , Front End Development (or closely related...weeks). At Fidelity, we value honesty, integrity, and the safety of our associates and customers within a heavily… more
    JobGet (05/02/24)
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  • Daiichi Sankyo, Inc. (Basking Ridge, NJ)
    …to epidemiology strategy for assigned products. Collaborate with epidemiology colleagues and Product Safety Lead to identify research gaps, develop protocols, ... study design, preparation of data for statistical analysis to obtain background rates) for development of safety documents (eg, RMP), support SMTs, SERM or other… more
    HireLifeScience (04/04/24)
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