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Key Responsibilities:
- Manage the complete IRB meeting workflow, from review of submissions to post-meeting documentation.
- Act as the central liaison between clients, Board members, and internal teams.
- Ensure all consent forms meet regulatory standards through thorough pre-reviews.
Requirements:
- Bachelor's degree and at least 2 years of IRB experience, or equivalent.
- Certified IRB Professional (CIP) certification required within one year of eligibility.
- Advanced knowledge of federal human-subject protection regulations strongly preferred.
Benefits:
- Fully remote position with a competitive base salary of $66,767–$116,089.
- Health coverage, paid holidays, and additional time-off benefits.
- Opportunities for professional development through conferences, webinars, and training.
Partner Company
The company coordinates Institutional Review Board (IRB) meetings within a highly regulated clinical research environment. They offer a collaborative and inclusive culture focused on ethical, patient-centered outcomes, though company size is not specified.