Clinical Coordinator
New
T
Tiny HealthBiotech Microbiome
North America, Core hours are 9am–6pm CST, shiftable by up to two hours either wayFull-TimeMiddle
Salary not disclosed
Apply NowOpens the employer's application page
Job Details
- Experience
- 2+ years
- Required Skills
- Project ManagementHIPAA
Requirements
- Bachelor’s degree in life sciences, public health, clinical research, or a related field
- 2+ years of experience in clinical research coordination, clinical operations, or a related role
- Familiarity with IRB processes and human subjects research requirements
- Strong organizational skills and attention to detail across multiple concurrent projects
- Ability to manage timelines, documentation, and stakeholder communication effectively
- Comfort working in a fast-moving, early-stage environment with evolving processes
- Excellent written and verbal communication skills
- Previous experience in a fast-paced startup environment
Responsibilities
- Support the day-to-day coordination of observational, interventional, and real-world evidence studies
- Assist with study startup activities, including site onboarding, documentation, and timeline tracking
- Maintain study schedules, task plans, and internal communication across stakeholders
- Coordinate sample logistics, participant workflows, and data collection processes
- Support IRB submissions, amendments, and continuing reviews in partnership with study leadership
- Maintain accurate study documentation, including protocol files, consent forms, and essential trial documents
- Partner with internal Science, Bioinformatics, and Product teams to support metadata capture and study execution
- Assist with clinical study reporting, including progress updates, interim summaries, and final documentation
View Full Description & ApplyYou'll be redirected to the employer's site
