• Director, HARP Care Management

    Healthfirst (NY)
    …related to behavioral health programs, including the launch of new products or regulatory initiatives + Act as a public-facing clinical leader with community ... in a health plan or integrated delivery system + Demonstrated experience with regulatory compliance, clinical quality improvement, and care management + Advanced… more
    Healthfirst (07/25/25)
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  • Quality Monitoring Coordinator-Environmental…

    Mount Sinai Health System (New York, NY)
    …field + 3 years experience **Responsibilities** + Ensures compliance with good clinical practice and regulatory guidelines. + Completes and coordinates ... monitoring responsibilities in strict adherence to regulatory requirements, standards and protocols. + Responsible for a...comparison review of collected data and scans of original clinical consent documents that are sent to the Data… more
    Mount Sinai Health System (08/16/25)
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  • Principal, Strategic Consulting, Patient Centered…

    IQVIA (New York, NY)
    …experience in PCS/Patient Centered Outcomes research projects and knowledge of Clinical Outcome Assessments regulatory and scientific guidelines + Well-developed ... Strategy Consulting, Patient Centered Solutions** IQVIA provides scientific services spanning clinical trials, real world evidence, and consulting in all areas of… more
    IQVIA (06/24/25)
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  • Program Manager I - Permanency Resource Centers

    Hillside Family of Agencies (NY)
    …of the program including budget development and management, utilization, hiring training, clinical oversight, regulatory compliance, and safety of youth families ... individuals. + Community Based develops and maintains positive funder and regulatory relationships via effective communications and a pro-active approach in working… more
    Hillside Family of Agencies (08/19/25)
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  • Associate Director, Quantitative Pharmacology,…

    Otsuka America Pharmaceutical Inc. (Albany, NY)
    …**population PK and PK/PD analyses** . + Author **pharmacometrics sections** of clinical pharmacology documents for regulatory filings including annual reports, ... NLME** , **Julia, R, etc.** + Excellent working knowledge of phase I clinical operations, drug development, multi-region regulatory requirements. + Good working… more
    Otsuka America Pharmaceutical Inc. (08/16/25)
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  • Associate Counsel, Patents

    The Estee Lauder Companies (Melville, NY)
    …+ Interact with various areas of the business including commercial brand teams, clinical , regulatory , manufacturing and supply chain, and transactional groups + ... Support US and non-U.S. litigation, oppositions, IPRs, or other judicial and non-judicial proceedings around the world + Develop and deliver training curriculum to promote IP culture and capabilities for R&D organization + Demonstrable aptitude for adopting… more
    The Estee Lauder Companies (08/08/25)
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  • Director, Laboratory Operations

    IQVIA (Ithaca, NY)
    …of Laboratory Operations, you will lead and oversee all aspects of clinical laboratory testing, ensuring regulatory compliance, operational excellence, and ... **What you'll be doing:** + Leading and managing daily operations of the clinical testing laboratory, ensuring compliance with all regulatory standards. +… more
    IQVIA (07/12/25)
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  • Laboratory Administrative Specialist

    SUNY Upstate Medical University (Syracuse, NY)
    … laboratories. The Administrative Specialist ensures smooth information flow between the lab, clinical staff, and regulatory bodies to optimize patient care and ... plays a critical role in supporting the operational efficiency and regulatory compliance of the in-house New York State-certified Physician Office Laboratory… more
    SUNY Upstate Medical University (08/08/25)
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  • Associate Medical Director, Pharmacovigilance…

    Sumitomo Pharma (Albany, NY)
    …reports + Knowledge of drug development in the pharmaceutical industry, including clinical research and global regulatory requirements + Experience managing ... products. + Conduct safety surveillance over product life cycle, reviewing clinical trial and post-marketing Individual Case Safety Reports (ICSRs), including… more
    Sumitomo Pharma (08/15/25)
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  • (Senior) Data Team Lead

    IQVIA (New York, NY)
    …a specific CDM task (eg, Subject Matter Expert (SME). Comply with Good Clinical Practices (GCPs), applicable regulatory guidelines, SOPs, policies, and, where ... ability to apply them in practice. + Knowledge of Good Clinical Practices and relevant regulatory guidelines. + Comprehensive understanding of clinical drug… more
    IQVIA (08/01/25)
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