• SR AD / Director, Pharmacometrics (Remote)

    Boehringer Ingelheim (Ridgefield, CT)
    …Monolix, R, SAS, PBPK software) + Proficient knowledge in clinical pharmacology, clinical drug development, MID3, and regulatory guidelines + Strong team player, ... Broad knowledge in other data science fields, clinical pharmacology, clinical drug development, MID3, and regulatory guidelines **Compensation:** This position,… more
    Boehringer Ingelheim (06/17/25)
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  • Senior Research Investigator, Clinical…

    Bristol Myers Squibb (Princeton, NJ)
    …and/or lead modeling and simulation plans * Collaborate on cross-functional drug development teams, regulatory submissions, and departmental **Experience ... the effects of formulation changes, as well as informing other critical drug development questions to influence company decisions. Furthermore, this department is… more
    Bristol Myers Squibb (07/16/25)
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  • Pharmacist Specialist

    UPMC (Pittsburgh, PA)
    …management, pharmacy automation, non-sterile drug packaging and compounding, drug discrepancy investigation and resolution, regulatory compliance, and risk ... in accordance with the Pennsylvania Pharmacy Practice Act, Federal Drug Laws, and other regulatory organizations. + Identify and report suspected adverse drug more
    UPMC (07/23/25)
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  • Open Rank Pharmacy School Assistant, Associate,…

    University of Maryland, Baltimore (Baltimore, MD)
    …ability to engage in the application of practical pharmacometric approaches to drug development and regulatory decisions. Develop quantitative disease models and ... of pharmacometrics or statistical analysis and apply techniques to drug development and regulatory decisions. Ensure validity and accuracy of data and compliance… more
    University of Maryland, Baltimore (06/18/25)
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  • Clinical QC Compliance Associate II

    AbbVie (North Chicago, IL)
    …or related experience in an area such as quality assurance, clinical research, drug development, medical writing, regulatory , or product support/R&D. + Working ... . Job Description + Conducts independent quality control reviews of regulatory , scientific, and clinical documents with applicable checklists by checking against… more
    AbbVie (06/02/25)
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  • Drug Testing Specimen Collector

    DATTCO (Middletown, CT)
    …off + Paid holidays + Flexible spending account Primary Responsibilities: + Quarterly drug specimen collections to fulfill our regulatory requirements to conduct ... Drug Testing Specimen Collector Department: School Bus Safety Location: Middletown, CT START YOUR APPLICATION… more
    DATTCO (07/09/25)
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  • Medical Physicist-Radiology Physics

    Stony Brook University (Stony Brook, NY)
    …the Joint Commission on the Accreditation of Health Care Organizations, Nuclear Regulatory Commission, Food and Drug Administration, and State Radiation Control ... (3) professional references. + Successfully complete a 4 panel drug screen * + Meet Regulatory Requirements for pre-employment screenings. + Provide a copy of… more
    Stony Brook University (07/15/25)
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  • Manager, Statistical Programming (Oncology)

    AbbVie (North Chicago, IL)
    …must have: (i) 5 years utilizing SAS programming concepts & techniques related to drug development & regulatory filings; (ii) 5 years applying CDISC standards, ... late stage development, interface with Statistics, Data Sciences, Medical Writing, Regulatory Publishing & Clinical Operations. + Develop & oversee development of… more
    AbbVie (05/09/25)
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  • Clinical Support Assistant - Microbiology Per Diem

    Stony Brook University (Stony Brook, NY)
    …a minimum of three (3) professional references. + Successfully complete a 4 panel drug screen * + Meet Regulatory Requirements for pre employment screenings. + ... include the following but are not limited to:** + Assist with the regulatory mandated inventory control process. All issues related to the lot numbers, shipments… more
    Stony Brook University (07/09/25)
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  • Data Analyst, Bureau of Tuberculosis Control

    City of New York (New York, NY)
    …and contribute to operational improvements across areas such as case management for drug -resistant TB, regulatory affairs, and the evaluation of newly arrived ... data from surveillance systems and electronic medical records. Assist the Regulatory Affairs Unit in drafting Commissioner's Orders for patients requiring legal… more
    City of New York (05/30/25)
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