• Oversight CRA

    Actalent (Brighton, MA)
    Clinical Research Associate Job Description We are seeking an experienced Oversight Clinical Research Associate to provide oversight ... management and reviewing trip reports of Clinical Research Associates (CRAs), as well as conducting CRA... Research Associates (CRAs), as well as conducting CRA performance assessments. Responsibilities + Provide oversight more
    Actalent (11/15/25)
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  • Sr. Clinical Research

    Parexel (Boston, MA)
    The Senior Clinical Research Associate (Sr. CRA ) is responsible for the site management, site monitoring and close-out of assigned clinical trials ... Practices (GCP), and the Sponsor's standards. The Sr. CRA is accountable for site management and monitoring, managing...+ Monitoring Experience: Minimum 3 years relevant experience in clinical research site monitoring (preferably 2 years… more
    Parexel (11/14/25)
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  • Senior Manager, Clinical Operations

    ConvaTec (Lexington, MA)
    …studies and provide input into budget forecasting activities. + Support the selection, oversight , and management of Clinical Research Organizations (CROs) ... closely with Clinical Study Managers (CSMs) and Clinical Research Associates (CRAs), manage all operational...partnership with the CRO and other vendors. + Provide oversight of study scope, quality, timelines, and budget with… more
    ConvaTec (09/19/25)
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  • Head of Ethics & Compliance Plasma Derived…

    Takeda Pharmaceuticals (Boston, MA)
    …shapes strategy, and fosters a culture of integrity. Key responsibilities include oversight of stakeholder interactions, clinical protocols, and medical plans; ... Reviews, assesses, and approves activities involving interactions with external stakeholders, clinical study protocols, and Medical Plans. + Leads the continuous… more
    Takeda Pharmaceuticals (10/09/25)
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