Clinical Research Coordinator

of experience in Clinical Research preferred

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

Proficiency in medical terminology and clinical documentation practices

to become a part of a team that’s changing the future of healthcare—one trial at a time.

Competitive pay (based on a combination of experience & education background) + 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

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