We're looking for an experienced Research Coordinator to join our team. You'll independently manage day-to-day trial activities, ensure regulatory compliance, and serve as a key point of contact for participants, investigators, and sponsors.
What you'll do
- Lead participant recruitment, screening, enrollment, and informed consent processes independently.
- Coordinate and conduct study visits, ensuring all procedures are carried out per protocol.
- Oversee data collection, entry, and quality control to maintain accuracy and integrity.
- Manage regulatory submissions, maintain IRB correspondence, and keep study files audit-ready.
- Oversee study supply inventory, kit preparation, and coordination of laboratory procedures.
- Manage participant communications, follow-up scheduling, and retention throughout the study.
- Collaborate with investigators, sponsors, and CROs; may mentor junior research staff.
What we're looking for
- Bachelor's degree in a health, science, or related field required.
- 2–4 years of clinical research experience, preferably in a coordinator role.
- CITI or GCP certification required; ACRP or SoCRA certification a plus.
- Working knowledge of FDA regulations, ICH guidelines, and IRB processes.
- Proficiency with EMR, CTMS, and electronic data capture (EDC) systems.
- Strong organizational skills with the ability to independently manage multiple active studies.
Why join us
- Lead studies across multiple phases of clinical research
- Clear pathway to senior coordinator and leadership roles
- Collaborative, mission-driven team environment
- Competitive salary, benefits, and professional development support
Ready to take the next step in your research career? Apply today.
Pay: $25.00 - $35.00 per hour
Benefits:
- 401(k)
- 401(k) matching
- Health insurance
- Paid time off
Work Location: In person
