Research Executive Assistant

Insight

  • Flint, Michigan
  • 16 days ago
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    Skills

    • Administrative Skillsunmatched
    • Budget Managementunmatched
    • Calendar Managementunmatched
    • Clinical Practices/Protocolsunmatched
    • Clinical Researchunmatched
    • Clinical Trialunmatched
    • Contract Research Organization (CRO)unmatched
    • Cross-Functionalunmatched
    • Document Managementunmatched
    • Documentationunmatched
    • Executive Assistant Skills unmatched
    • Leadershipunmatched
    • Microsoft Officeunmatched
    • Multitaskingunmatched
    • Operations Processesunmatched
    • Operations Researchunmatched
    • Organizational Skillsunmatched
    • Plan Meetingsunmatched
    • Regulationsunmatched
    • Regulatory Submissionsunmatched
    • Research Contractsunmatched
    • Startupunmatched
    • Systems Maintenanceunmatched
    • Time Managementunmatched
    • Travel Planningunmatched

    Description

    Insight Health Systems Clinical Research
    Research Executive Assistant
    Title: Research Executive Assistant – Clinical Research
    Location: Michigan- Flint or Dearborn (On-site required)
    Reports To: Chief Clinical Research Officer
    Schedule: Full-time, Monday–Friday, with flexibility for research-related deadlines
    Position Summary:
    The Research Executive Assistant provides high-level administrative, operational, and project
    coordination support to Insight Health System’s Clinical Research leadership. This role requires hands-on
    experience in clinical research/clinical Trials and a strong understanding of research workflows,
    regulatory timelines, sponsor interactions, and site operations. The Research Executive Assistant
    ensures seamless communication, efficient scheduling, and proactive support across a fast-paced
    research environment.
    Key Responsibilities:
    • Manage complex calendars, meeting coordination, and travel arrangements for research leadership
    • Prepare agendas, minutes, and follow-up action items for internal and external research meetings
    • Draft, edit, and format correspondence, presentations, and reports related to clinical research
    operations
    • Maintain confidentiality and handle sensitive information with discretion
    • Assist with research pipeline and study startup tasks such as feasibility coordination, document
    collection, and meeting scheduling
    • Support tracking of regulatory submissions, training logs, delegation logs, and study milestones
    • Coordinate sponsor and CRO visits, including SIVs, IMVs, and closeout meetings
    • Maintain organized filing systems for research documents, contracts, and communications
    • Track deadlines, deliverables, and cross-functional tasks across multiple studies
    • Support recruitment initiatives, community events, and research outreach activities
    • Assist with invoice tracking, budget documentation, and vendor coordination
    Minimum Qualifications:
    • Minimum 2–3 years of administrative experience in clinical Trials (required)
    • Strong understanding of Clinical Trials operations, regulatory processes, and sponsor interactions
    • Exceptional organizational, communication, and multitasking skills
    • Proficiency in Microsoft Office, CTMS platforms, and document management systems
    • Ability to work independently, anticipate needs, and manage competing priorities

    Numbers & Facts

    LocationFlint, Michigan
    WebsiteIINN.com

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