• Senior Representative, Regulatory

    Catalent Pharma Solutions (Bloomington, IN)
    **We're hiring for a Senior Regulatory Affairs Specialist to support compliance and regulatory affairs in Bloomington, Indiana!** Catalent is a ... mission: to help people live better, healthier lives. The ** Senior Regulatory Affairs Specialist** serves...+ Competitive salary with bonus potential. + Tuition reimbursement program . + Diverse, inclusive culture. + Generous 401K match.​… more
    Catalent Pharma Solutions (04/10/24)
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  • Senior Director- Global Medical…

    Lilly (IN)
    …"patient journey" and the strategic plan for the compound), medical support for regulatory affairs and interactions with government agencies (medical support for ... expertise, and relevant clinical experience, the Lilly Diabetes and Obesity - Medical Affairs Physician is an integral member of the medical affairs ,… more
    Lilly (05/08/24)
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  • Program Specialist

    Veterans Affairs, Veterans Health Administration (IN)
    …appropriate offices throughout the country and receive the necessary concurrence from senior VHA leadership and program oversight committees. Outline and ... with minimal guidance from management. Prepare and deliver complex briefings, reports and program updates to senior management and to the national program more
    Veterans Affairs, Veterans Health Administration (04/28/24)
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  • Senior Utilization Review Consultant (O-5…

    Immigration and Customs Enforcement (IN)
    …defined. Work is reviewed for feasibility, compatibility with other work, program / regulatory compliance, and effectiveness in meeting requirements or expected ... Assistant Director for Healthcare Compliance, Office of Health Plan Management. The Senior Utilization Review Consultant will report directly to the IHSC Regional… more
    Immigration and Customs Enforcement (05/04/24)
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  • Health Economics and Outcomes Research (HEOR)…

    ThermoFisher Scientific (Indianapolis, IN)
    …including dossier development and submissions, in collaboration with Medical & Scientific Affairs and Market Access colleagues. + Provide support and guidance to ... early-stage program teams with various RWE activities to optimize clinical...well as emerging HEOR/RWE methodologies and applications. + Communicate regulatory with internal and external stakeholders to ensure all… more
    ThermoFisher Scientific (02/17/24)
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  • Management and Program Analyst

    Veterans Benefits Administration (IN)
    …Oversight (OPO). OPO administers the programs and activities for ten business lines/ program offices within the Department of Veterans Affairs , Veterans Benefits ... or anticipated problems, communicates with managers, and provides consultation on program administration matters. Provides comprehensive briefings to senior more
    Veterans Benefits Administration (05/03/24)
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  • Associate Director, GMP Quality Control

    Sumitomo Pharma (Indianapolis, IN)
    …changes to contract manufacturing organizations, testing laboratories, clinical sites and regulatory affairs as needed. + Responsible for compliance with ... Director ensures compliance with GMPs, SMPA procedures and applicable global Regulatory guidelines by providing oversight and management of the global contract… more
    Sumitomo Pharma (04/19/24)
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  • Landfill Operations Management Trainee

    WM (Danville, IN)
    …Management Trainee (DOMT) position is part of a required developmental training program lasting up to 18 months.** The duties and responsibilities are under ... leachate management, and waste streams and sales. The Disposal OMT training program is designed to develop individuals into Operations Managers and District Managers… more
    WM (02/23/24)
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  • Sr Director - Medicines Quality Organization, Cell…

    Lilly (Indianapolis, IN)
    …operate across many corporate functions including Global Patient Safety (GPS), Global Regulatory Affairs (GRA), Clinical Design, Delivery and Analytics (CDDA), ... Organization (MQO) is for the design, implementation, and execution of a medical, regulatory , and safety quality system to support the evolving cell and gene therapy… more
    Lilly (04/11/24)
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  • Dermatology Thought Leader Liaison

    AbbVie (Indianapolis, IN)
    …and internal departments including Agency Partners, Marketing, Market Research, Legal, Regulatory , Medical Affairs , Office of Ethics and Compliance, Consumer ... for national and regional conference product theaters + Uncover regional speaker program opportunities based on local market dynamics, provide guidance on speaker… more
    AbbVie (05/01/24)
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  • SVP, Risk Adjustment Operations…

    Humana (Indianapolis, IN)
    …support regulation impacts to existing programs and helps to ensure any new program changes are implemented with changing regulatory landscape. Develops the ... join the Healthcare Quality Reporting and Improvement (HQRI) organization as Senior Vice President (SVP), Risk Adjustment Operations and Interoperability. This key… more
    Humana (05/08/24)
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  • Supervisory Human Resources Specialist (Rec/Place)

    Deputy Assistant Secretary for Information and Technology (IN)
    …and providing oversight for a complex nationwide federal recruitment and placement program ; participating as a senior recruitment and placement consultant in ... received, whichever comes first. This position is in the Department of Veterans Affairs , Office of Information and Technology (OIT), Office of People Science (OPS),… more
    Deputy Assistant Secretary for Information and Technology (05/08/24)
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