• Eisai, Inc (Charlotte, NC)
    …to work cross-functionally while adhering to all of Eisai's ethics and compliance standards. Senior Neurology Account Specialist (Sr NAS) Responsibilities ... Alzheimer's disease (AD) or mild AD. TheSenior Neurology Account Specialist (Sr NAS) will be part of a diverse...the primary role of demand generation by conveying complex clinical information to customers and key stakeholders consistent with… more
    HireLifeScience (09/17/24)
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  • Merck & Co. (North Wales, PA)
    Job DescriptionTh e Health Literacy Specialist role in the Medical Writing & Disclosure (MW&D) department will be primarily responsible for preparing Plain Language ... (PLS), including the Protocol PLS and Results PLS, of clinical studies per our company's process es and standards...per our company's process es and standards to ensure compliance with internal policy, regulatory requirements, and health literacy… more
    HireLifeScience (09/05/24)
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  • Merck & Co. (Rahway, NJ)
    …located in Rahway, New Jersey includes a state-of-the-art sterile drug product cGMP clinical supply manufacturing facility known as FLEx Sterile that is currently in ... major role in the long-term success of delivering our clinical pipeline to patients across the globe throughout a...drug conjugates (ADCs), in addition to others.- --The Senior Specialist , Engineering will serve as a business representative in… more
    HireLifeScience (09/10/24)
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  • Eisai, Inc (San Diego, CA)
    …/ safe administration by working with appropriate Health Care Providers. Complete ongoing clinical acumen and compliance training with goal of being expert level ... customer business, disease state, product prescribing information, approved promotional clinical trials, patient access to medication, and regulatory/ compliance more
    HireLifeScience (08/27/24)
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  • Eisai, Inc (Louisville, KY)
    …/ safe administration by working with appropriate Health Care Providers. Complete ongoing clinical acumen and compliance training with goal of being expert level ... customer business, disease state, product prescribing information, approved promotional clinical trials, patient access to medication, and regulatory/ compliance more
    HireLifeScience (08/28/24)
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  • Merck & Co. (Rahway, NJ)
    Job DescriptionPosition Description: Specialist , Environmental, Health, and Safety (EHS) As a member of the Site Environmental, Health, and Safety (EHS) team, work ... Rahway site.Integrates EHS programs into daily operations to assure regulatory compliance , continuous improvement and performance objectives are met around EHS.… more
    HireLifeScience (09/06/24)
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  • Legend Biotech USA, Inc. (Raritan, NJ)
    …an immunotherapy in the treatment of multiple myeloma.Legend Biotech is seeking Maintenance Specialist as part of the Technical Operations team based in Raritan, New ... be responsible for maintenance support and mechanical system operations for cGMP Clinical and Commercial Cell Therapy Manufacturing on a modified second shift. This… more
    HireLifeScience (08/29/24)
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  • Legend Biotech USA, Inc. (Raritan, NJ)
    …an aseptic manufacturing facility, preferably in quality assurance, manufacturing compliance , clinical quality, technical operations or cell therapy.Experience ... multiple myeloma.Legend Biotech is seeking a QA Shop Floor Specialist as part of the Quality Operations team based...oversight of the production of autologous CAR-T products for clinical trials and commercial operation in a controlled cGMP… more
    HireLifeScience (07/26/24)
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  • Legend Biotech USA, Inc. (Raritan, NJ)
    …of multiple myeloma.Legend Biotech is seeking a QA Warehouse Incoming Raw Material Specialist as part of the Quality team based in Raritan, NJ. Role OverviewThe ... QA Warehouse Incoming/Raw Material Specialist is an exempt level position with responsibility to...materials related to manufacturing of autologous CAR-T products for clinical trials and commercial operation in a controlled cGMP… more
    HireLifeScience (08/14/24)
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  • Legend Biotech USA, Inc. (Raritan, NJ)
    …in an aseptic manufacturing facility, preferably in quality assurance, manufacturing compliance , clinical quality, or cell therapy.Knowledge of cGMP regulations ... of multiple myeloma.Legend Biotech is seeking QA Lab Oversight Specialist as part of the Quality team based in...the site Quality Control laboratories responsible for testing of pre- clinical , clinical , and commercial stage CAR-T cellular… more
    HireLifeScience (07/26/24)
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  • Legend Biotech USA, Inc. (Raritan, NJ)
    …in the treatment of multiple myeloma.Legend Biotech is seeking Change Control Specialist as part of the Technical Operations team based in Raritan. Role ... OverviewThe Change Control Specialist will be part of the Technical Operations team...support for the production of autologous CAR-T products for clinical trials and commercial operation in a controlled cGMP… more
    HireLifeScience (08/17/24)
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  • Legend Biotech USA, Inc. (Raritan, NJ)
    …has experience working in a cGMP manufacturing facility, quality assurance, manufacturing compliance , clinical quality, or cell therapy. GxP Quality System ... of multiple myeloma.Legend Biotech is seeking QA Document Control Specialist as part of the Quality team based in...within a cell therapy manufacturing facility to support both clinical and commercial requirements in a sterile GMP environment.… more
    HireLifeScience (07/26/24)
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  • Legend Biotech USA, Inc. (Raritan, NJ)
    …in the treatment of multiple myeloma.Legend Biotech is seeking a Technical Equipment Specialist as part of the Technical Operations team based in Raritan, NJ. Role ... OverviewThe Technical Equipment Specialist will be responsible for ensuring equipment/systems required to...of the CAR-T Equipment team in support of on-going clinical and commercial manufacturing as well as facility expansions… more
    HireLifeScience (07/26/24)
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  • Novo Nordisk Inc. (West Lebanon, IN)
    …reviews of manufacturing and support documentation and records to certify compliance with in-house specifications/standards and GMP for all NNUSBPI products. This ... Essential Functions Reviews all manufacturing and support records to certify compliance with specifications and procedures Releases product based on Quality… more
    HireLifeScience (08/24/24)
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  • Interim HealthCare (Columbia, SC)
    …caregivers in a way that raises the caliber of home-based care. As the Clinical Quality Specialist - Registered Nurse (RN) for Interim HealthCare, you'll play ... healthcare since 1966. We are currently hiring a Hospice Clinical Quality Specialist - Registered Nurse (RN)...of improvement.Complete data collection and analysis to ensure regulatory compliance related to the Home Health agency clinical more
    JobGet (09/18/24)
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  • Blanchard Valley Hospital (Findlay, OH)
    PURPOSE OF THIS POSITION The primary purpose of the RN Clinical Specialist - Value Analysis position is to coordinate, communicate, and ensure quality, cost ... the organization. Duty 3: Reviews and maintains market share compliance information for clinical contracts that have these requirements. Has a working knowledge… more
    JobGet (09/15/24)
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  • Careerbuilder-US (Pomona, CA)
    …with a rapidly growing, national healthcare equipment company to seek out a full-time Clinical Asset Specialist for their new office in Pomona, CA! If you ... and strong capabilities in Microsoft Office, APPLY TODAY! Responsibilities: Oversees clinical equipment projects and initiatives for the facility. Analyzes trends,… more
    JobGet (09/15/24)
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  • The Staff Pad (Helena, MT)
    …they relate to revenue capture. Lastly, this position supports the corporate compliance program by verifying adherence to charge posting policies and procedures by ... ensuring that the charge master is in compliance with all applicable regulatory guidelines. This position oversees staff members as part of the revenue integrity… more
    JobGet (09/19/24)
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  • DivIHN Integration Inc (Atlanta, GA)
    …Essential Duties and Responsibilities: With oversight, develops high quality clinical documents ensuring scientific excellence and regulatory compliance . ... documents per regulations, manuscripts/abstracts for publication and/or presentation. Ensure compliance of clinical documents with national and international… more
    JobGet (09/15/24)
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  • The Staff Pad (Helena, MT)
    …orCurrent ASCP licensure as a Clinical Laboratory Scientist (CLS) or Clinical Laboratory Specialist (CLSp) required for Main and North Lab Technical ... setting the gold standard for healthcare in Montana.Job Title: Technical Clinical Laboratory SupervisorJob Summary: The Technical Clinical Laboratory Supervisor… more
    JobGet (09/19/24)
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