Clinical Research Coordinator I, II, or III

Previous experience as a Clinical Research Coordinator required

Industry-sponsored trial experience strongly preferred (vaccine study experience a plus)

Familiarity with electronic data capture (EDC), IVRS, and other trial platforms

Deep understanding of FDA, ICH-GCP regulations, and clinical trial procedures

Proficiency in medical terminology and clinical documentation practices

Competitive pay + annual performance incentives

Medical, dental, and vision insurance

401(k) plan with company match

Paid time off (PTO) and company holidays

A mission-driven culture focused on advancing medicine and improving patient outcomes

You’ll be part of a growing, mission-driven organization that values its people. At our core, we’re committed to bringing innovative medical treatments to patients faster—while creating an environment where employees thrive. If you’re passionate about clinical research and ready to make a difference, we’d love to hear from you.

Coordinate all aspects of assigned clinical trials from site initiation to study close-out

Maintain compliance with study protocols, GCP/ICH guidelines, FDA regulations, IRB policies, and company SOPs

Manage subject recruitment, informed consent, and retention strategies

Ensure timely data entry and resolution of EDC queries

Report and follow up on all adverse events, serious adverse events, and deviations

Collaborate with investigators, lab teams, sponsors/CROs, and internal stakeholders