• HCP Marketer

    Chiesi (Cary, NC)
    About us Based in Parma, Italy, Chiesi is an international research-focused pharmaceuticals and healthcare group with 90 years' experience, operating in 30 countries ... of goals and an eye towards innovation. + Ensure compliance with regulatory , legal, and corporate requirements both separately and for respiratory patients +… more
    Chiesi (05/24/25)
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  • Clinical Trial Assistant

    IQVIA (Durham, NC)
    regulatory requirements, ie, Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines as provided in company training. ... daily administrative activities, in conjunction with the Clinical Research Associates and Regulatory and Start-Up teams, to ensure a complete and accurate Trial… more
    IQVIA (05/24/25)
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  • Field Evaluations Engineer - Northeast Region

    UL, LLC (Raleigh, NC)
    Conduct on site engineering evaluations to help regulatory authorities determine the compliance of a product, leading to "approval" of the installation. The ... Projects include frequent travel to conduct on-site product evaluations. Some International travel required. + Initiates communication with clients and AHJ's to… more
    UL, LLC (05/23/25)
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  • Lead, HCP Marketer

    Chiesi (Cary, NC)
    About us Based in Parma, Italy, Chiesi is an international research-focused pharmaceuticals and healthcare group with 90 years' experience, operating in 30 countries ... achievement of goals and an eye towards innovation. + Ensure compliance with regulatory , legal, and corporate requirements both separately and for asthma and copd… more
    Chiesi (05/17/25)
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  • Senior Patient Marketer

    Chiesi (Cary, NC)
    About us Based in Parma, Italy, Chiesi is an international research-focused pharmaceuticals and healthcare group with 90 years' experience, operating in 30 countries ... meetings, events, and other activities as needed + Ensure compliance with regulatory , legal, and corporate requirements both separately and for the sickle cell… more
    Chiesi (05/17/25)
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  • QA Representative - Warehouse 2nd Shift

    Lilly (Durham, NC)
    …support during preparation for Pre-Approval/General Inspections by various regulatory agencies. **Key Objectives/Deliverables:** + Responsible for adhering to ... + Participate in self-led inspections and provide support during internal / external regulatory inspections. + Effectively review and / or redline to ensure quality… more
    Lilly (05/15/25)
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  • Accounting Advisory Manager

    Grant Thornton (Charlotte, NC)
    …on complex accounting transactions. You will help clients address their transactional, regulatory , and strategic needs - all with the resources, environment, and ... you excel. More specifically, support on complex accounting matters arising from regulatory or strategic business changes such as adoption of new accounting… more
    Grant Thornton (05/14/25)
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  • Sr. Director - Health, Safety, Environmental

    Lilly (Durham, NC)
    …for the RTP site. Responsibilities will include but not limited to: Ensuring regulatory / site / corporate HSE compliance, development of HSE systems / processes ... the HSE management system. + Achieving environmental goals. + Permitting, regulatory compliance, and building relationships with HSE regulators. + Partnering with… more
    Lilly (05/13/25)
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  • Associate - QA Compliance - CSV and DI

    Lilly (Durham, NC)
    …candidate will utilize Computer System Validation methodologies to ensure regulatory compliance, consistency, and sustainment. Key responsibilities include ensuring ... ensuring that all processes are aligned with corporate and regulatory requirements. **Key Objectives/Deliverables/Responsibilities** : + Ensure RTP's computer system… more
    Lilly (05/09/25)
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  • Medical Director(Hematology/Oncology) - Remote US

    ThermoFisher Scientific (Wilmington, NC)
    …trials, oversee case-processing activities through all phases of development and perform regulatory reporting and medical monitoring. As part of your work with ... trials to ensure company SOPs, client directives, good clinical practice, and regulatory requirements are followed. Attends and presents at investigator and sponsor… more
    ThermoFisher Scientific (05/08/25)
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