Research Executive Assistant
Listed on 2026-07-31
-
Administrative/Clerical
Office Administrator/ Coordinator
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 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
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