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Responsibilities:
- Coordinate day-to-day clinical study execution, including site onboarding, documentation, and timeline tracking.
- Support IRB submissions, amendments, and maintain study documentation for regulatory compliance.
- Partner cross-functionally with science, bioinformatics, and product teams to ensure study operations.
Qualifications:
- Bachelor’s degree in life sciences or related field and 2+ years of clinical research coordination experience.
- Familiarity with IRB processes and strong organizational skills.
- Comfort working in a fast-paced startup environment with excellent communication.
How We Work:
- Remote-first culture with core hours 9am-6pm CST, shiftable by up to two hours.
- Written communication first, then huddles, meetings as last resort.
- Fast but careful: we move quickly but double-check all health-related work.
Tiny Health
Tiny Health advances lifelong health through precision microbiome science using shotgun metagenomics and AI. Founded in 2020, it is a remote-first startup with a diverse international team focused on making the microbiome measurable and actionable.