• Principal Biostatistician FSP, Neuroscience

    IQVIA (Durham, NC)
    …get all the benefits of working for an industry leading global CRO while collaborating directly with expert cross-functional sponsor teams. Sponsor clients include ... world class pharmaceutical and biotech companies offering you unique opportunities to...+ Write statistical analysis plans. + Monitor internal and CRO project activities including timelines, deliverables, and availability of… more
    IQVIA (07/10/25)
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  • Associate Director, Data Sciences, Safety,…

    IQVIA (Durham, NC)
    …Degree + 10 years related experience, including 3 years of relevant industry ( CRO / Pharmaceutical ) and/or sales experience Req Or + Equivalent combination of ... + General knowledge of the Clinical Development space, Clinical Research Organization ( CRO ) operations, are required. + Sales experience in a Clinical Research… more
    IQVIA (07/02/25)
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  • QA Specialist I - Document Control

    Charles River Laboratories (Rockville, MD)
    …off-site archive facilities for data storage and retrieval, as required + Ensure the Document Control room is in order + Assist in compiling Document Control ... can feel passionate about. **Job Summary** The QA Specialist I - Document Control is responsible for managing all controlled GMP documentation in compliance with… more
    Charles River Laboratories (09/24/25)
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  • CSV Specialist I

    Charles River Laboratories (Memphis, TN)
    …of experience in computer system validation within a regulated industry ( pharmaceutical , medical device, biotechnology). * An equivalent combination of education and ... Development and Manufacturing Organization (CDMO) group supports biotechnology and pharmaceutical companies in advancing their complex programs from early… more
    Charles River Laboratories (09/21/25)
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  • Manager, CSV & Data Integrity

    Charles River Laboratories (Memphis, TN)
    …years of experience in computer system validation within a regulated industry ( pharmaceutical , medical device, biotechnology). * Minimum of 5 years of experience ... Development and Manufacturing Organization (CDMO) group supports biotechnology and pharmaceutical companies in advancing their complex programs from early… more
    Charles River Laboratories (09/20/25)
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  • Clinical Research Specialist - The Angeles Clinic…

    Cedars-Sinai (Los Angeles, CA)
    …in IRB clinical research application procedures preferred. Related experience in Pharmaceutical /Biotechnology, or Contract Research Organization ( CRO ). + 5 years ... where applicable. + Acts as a liaison with Principal Investigators, pharmaceutical company representatives and other project funding organizations to monitor and… more
    Cedars-Sinai (09/20/25)
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  • Medical Director, US Medical Affairs

    J&J Family of Companies (Horsham, PA)
    …in pharmaceutical trial design and conduct (Phases II-IV) within the pharmaceutical industry, CRO or academia is preferred. + Excellent written, oral ... preferred + A minimum of five years of relevant experience in the pharmaceutical industry or equivalent experience is preferred + Experience developing and executing… more
    J&J Family of Companies (09/20/25)
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  • Manufacturing Associate I

    Charles River Laboratories (Northridge, CA)
    …the highest quality cellular material and services to biotech and pharmaceutical companies and research organizations that are performing innovative research and ... incubator ID, batch number, and microbiological identification outside of clean room . Performs per-batch personnel monitoring on each sterile staff member. Performs… more
    Charles River Laboratories (09/17/25)
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  • Director, Technical Operations

    Charles River Laboratories (Northridge, CA)
    …the highest quality cellular material and services to biotech and pharmaceutical companies and research organizations that are performing innovative research and ... multiple complex projects to drive revenue growth initiatives (eg. Donor Room Operations/ Donor Base Optimization, Technical Operations, custom projects), working… more
    Charles River Laboratories (09/17/25)
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  • Associate Director Production Quality

    Charles River Laboratories (Rockville, MD)
    …to and ensure necessary Quality oversight to areas within span of control . + Effectively model, demonstrate and live an employee-focused leadership style that ... + Minimum 8 years of experience in a biologics, pharmaceutical , medical device, or related industry. 10 years of...and EP guidelines and regulations associated with the quality control of biologic/cell therapies + Experience preferred with CDMO… more
    Charles River Laboratories (09/11/25)
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