• Merck & Co. (Rahway, NJ)
    …processes/ methods in conformance to all applicable regulatory requirements, regulatory filings and company policies.The Associate Director also ensures that ... Job DescriptionThe Associate Director , ESQL is responsible for all activities at...and technical advice, counseling to site leadership, and on-site supervision . The AD may serve as a subject matter… more
    HireLifeScience (05/25/24)
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  • Merck & Co. (Rahway, NJ)
    …The Associate Director will perform job duties independently with minimal supervision and/or lead QP2 efforts on drug/vaccine development programs, and author or ... development (MIDD) to routinely enable efficient drug discovery/development and/or regulatory decisions. The Pharmacometrics group within QP2 brings an experienced… more
    HireLifeScience (05/02/24)
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  • Eisai, Inc (Nutley, NJ)
    …to hear from you. Job Summary: As the Americas IT Security and Compliance Director , you play a pivotal role in ensuring the organization's adherence to security, ... regulatory , and compliance standards. Collaborating with business and EIT stakeholders, you promote awareness of best practices and strengthen compliance with GDPR,… more
    HireLifeScience (05/25/24)
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  • Daiichi Sankyo, Inc. (Basking Ridge, NJ)
    …. This position provides input to entire drug development plans with minimal supervision and authors regulatory responses and other documents with minimal ... programmers and statisticians. Additionally, this position works under minimal supervision to solve complex project problems.Responsibilities- Protocol Development, Statistical… more
    HireLifeScience (05/25/24)
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  • Daiichi Sankyo, Inc. (Basking Ridge, NJ)
    …Ensure timely and accurate completion of AI/ML deliverables- Contribute, with limited supervision , to documents submitted to regulatory or pricing authorities- ... management.Responsibilities Project level AI/ML activities - Responsible, with limited supervision , for both managing and implementing AI/ML projects from business… more
    HireLifeScience (05/24/24)
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  • Daiichi Sankyo, Inc. (Basking Ridge, NJ)
    …quality standards and timelines and that quality of data is suitable for regulatory submission. The Associate Director will have routine interaction with key ... Directive, and International Conference on Harmonization (ICH) guidelines. The Associate Director is accountable for operational planning and execution at the study… more
    HireLifeScience (05/18/24)
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  • Daiichi Sankyo, Inc. (Basking Ridge, NJ)
    …to budget and accurate completion of Statistical deliverables. Contribute, with limited supervision , to documents submitted to Regulatory or Pricing Authorities. ... cross-functional Study team(s).Responsibilities- Study Responsibility - Responsible, with limited supervision , for study activities assigned, eg for a clinical… more
    HireLifeScience (05/17/24)
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  • Daiichi Sankyo, Inc. (Basking Ridge, NJ)
    …opportunity employer including veterans and people with disabilities.SummaryThe Associate Director will be responsible for developing and implementing Clinical ... hands on population PK and PKPD analyses and participate in regulatory interactions and submissions representing the Clinical Pharmacology and Pharmacometrics/… more
    HireLifeScience (04/23/24)
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  • Daiichi Sankyo, Inc. (Basking Ridge, NJ)
    …function on study and project teams, and participate in and contribute to regulatory and KOL meetings. This position requires significant understanding of PK-PD and ... Pop PK-PD concepts and analysis, phase 1-4 clinical studies, literature, regulatory guidelines, and physiological/pharmacological aspects of the drug. This position… more
    HireLifeScience (05/01/24)
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  • Daiichi Sankyo, Inc. (Basking Ridge, NJ)
    …that all key stakeholders are fully on board. Requires minimal supervision . Proactively predicts and prevents issues and conflicts; appropriately escalates as ... Demonstrates strong knowledge of the industry, vendor base, and regulatory issues for respective categories. Leads the development of sourcing… more
    HireLifeScience (05/09/24)
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  • Daiichi Sankyo, Inc. (Basking Ridge, NJ)
    …in study design, statistical analysis and interpretation of results with some supervision . This position contributes to specific aspects of drug development plans ... with minimal supervision and contributes to documents submitted to Health Authorities...phase of the development are scientifically sound, can fulfill regulatory requirements and deliver the pre-specified product profile.- CRO… more
    HireLifeScience (04/04/24)
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  • Novo Nordisk Inc. (Plainsboro, NJ)
    About the Department The Clinical, Medical and Regulatory (CMR) department at Novo Nordisk is one of the most diverse and collaborative groups within the ... organization. From health-care-provider interactions and developing and implementing regulatory strategies with the FDA to providing medical education and collecting… more
    HireLifeScience (05/23/24)
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  • Novo Nordisk Inc. (Plainsboro, NJ)
    regulatory agencies. Supervise designated personnel. Relationships Report to the Director /Associate Director /Lead Regulatory Scientist/Sr. Manager ... About the Department The Clinical, Medical and Regulatory (CMR) department at Novo Nordisk is one of the most diverse and collaborative groups within the… more
    HireLifeScience (05/21/24)
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  • Regulatory Interpretations Director

    US Bank (New York, NY)
    …years of progressive experience in financial services, banking, accounting policy, or regulatory supervision . - Strong knowledge of audit, risk management, ... proposed new activities or transactions - Direct experience in regulatory policy making or large bank supervision ...in regulatory policy making or large bank supervision function at regulatory banking agency -… more
    US Bank (05/22/24)
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  • Assistant Director of Facilities Operations…

    New York State Civil Service (Old Westbury, NY)
    …and evaluation for the development and success of assigned personnel.Assists the Director in the overall supervision of the Facilities Department. Ability ... NY HELP No Agency SUNY Old Westbury Title Assistant Director of Facilities Operations - Custodial and Maintenance Occupational Category Skilled Craft,… more
    New York State Civil Service (04/30/24)
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  • Program Director (Mica Shelter)

    Acacia Network (New York, NY)
    …3877 Job Category: Transitional Housing Position Type: Full Time Details: Under supervision of the Program Administrator, the Program Director ensures quality ... the purpose of meeting the physical, emotional and social needs of clients. The Program Director provides supervision to the intake services and works with the … more
    Acacia Network (04/19/24)
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  • Assistant Program Director

    Acacia Network (Queens, NY)
    …meeting the physical, emotional, and social needs of clients. The Assistant Program Director provides supervision to the Intake Services and Case Management ... Transitional Housing Assistant Program Director Queens, Bronx, Brooklyn, Manhattan, NY : 2/5/2024...shelter's Clinical and Social Services functions according to DHS regulatory and accreditation requirements. This individual is responsible for… more
    Acacia Network (05/06/24)
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  • Program Director (MICA Shelter)

    Acacia Network (Bronx, NY)
    …3537 Job Category: Transitional Housing Position Type: Full Time Details: Under supervision of the Program Administration, the Program Director ensures quality ... Transitional Housing Program Director (MICA Shelter) Bronx, NY : 4/13/2023 Job...the 200 bed MICA population shelter according to DHS regulatory and accreditation requirements. This individual is responsible for… more
    Acacia Network (04/16/24)
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  • Program Director

    Acacia Network (Bronx, NY)
    …ID#: 3538 Job Category: Promesa Housing Position Type: Full Time Details: Under supervision of the Program Administrator, the Program Director (Homes Together ... of meeting the physical, emotional, and social needs of clients. The Program Director provides supervision of all programs' services and works to develop,… more
    Acacia Network (04/16/24)
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  • Medical/Scientific Director , Medical…

    AbbVie (Florham Park, NJ)
    …level will be determined by the qualifications listed below. The Medical/Scientific Director , Medical Affairs - Psychiatry Pipeline is a strategic scientific expert ... with external stakeholders, including key opinion leaders, academic institutions, and regulatory agencies. + Lead the development and execution of scientific… more
    AbbVie (05/23/24)
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