Research Coordinator

Required Skills & Experience

Must-Haves:

Experience in clinical research, research administration, biotech, pharmaceuticals, or a university research environment Hands-on exposure to compliance within clinical research Experience working with human-subject research and/or research data collection Understanding of IRB (Institutional Review Board) processes and requirements Experience preparing or submitting documentation to an IRB Strong administrative skills and comfortable in a behind-the-scenes, documentation-heavy support role Detail-oriented and able to pick up new processes and systems quickly Experience supporting research studies from an administrative or compliance perspective

Plusses:

Previous Meta experience or familiarity with Meta systems/processes Previous Research Assistant or Study Coordinator experience Biotech or pharmaceutical industry experience Experience working with clinical research grants Paralegal or law office background, particularly involving compliance or document-heavy work Experience across both university/academic research and industry environments Direct experience managing IRB submissions

Day-to-Day:

Provide behind-the-scenes administrative and compliance support for research activities Prepare, organize, and submit documentation to the IRB Support compliance requirements associated with human-subject research and data collection Maintain accurate research, regulatory, and compliance documentation Assist research teams with administrative processes throughout the study lifecycle Coordinate documentation and submissions across internal teams and third-party review organizations Navigate internal systems and quickly learn established processes Handle a significant volume of documentation, submissions, and process-driven administrative work Ensure research activities and documentation align with applicable compliance requirements Support study coordinators, researchers, and other stakeholders as needed

Job Description:

Insight Global is seeking a Clinical Research Compliance / IRB Support professional for a top technology client. This individual will provide critical behind-the-scenes support for research activities involving human subjects, with a strong focus on compliance, documentation, and IRB submissions. The ideal candidate has experience within clinical research, biotech, pharmaceuticals, academic research, or a related compliance-driven environment and understands the processes surrounding human-subject research and data collection. This role is highly administrative and process-oriented, so the ideal candidate will be detail-focused, comfortable managing documentation, and able to learn new systems quickly. Candidates with previous Research Assistant, Study Coordinator, paralegal, biotech, or clinical research compliance experience would translate especially well.

Nice to Have Skills & Experience

Plusses:

Previous Meta experience or familiarity with Meta systems/processes Previous Research Assistant or Study Coordinator experience Biotech or pharmaceutical industry experience Experience working with clinical research grants Paralegal or law office background, particularly involving compliance or document-heavy work Experience across both university/academic research and industry environments Direct experience managing IRB submissions

Job Description

Insight Global is seeking a Clinical Research Compliance / IRB Support professional for a top technology client. This individual will provide critical behind-the-scenes support for research activities involving human subjects, with a strong focus on compliance, documentation, and IRB submissions. The ideal candidate has experience within clinical research, biotech, pharmaceuticals, academic research, or a related compliance-driven environment and understands the processes surrounding human-subject research and data collection. This role is highly administrative and process-oriented, so the ideal candidate will be detail-focused, comfortable managing documentation, and able to learn new systems quickly. Candidates with previous Research Assistant, Study Coordinator, paralegal, biotech, or clinical research compliance experience would translate especially well.