Clinical Research Coordinator

Job Summary

Supporting the Clinical Research Team in a full-time remote capacity, the Clinical Research Coordinator will manage day-to-day study operations, track enrollment and participant flow, and ensure adherence to clinical research protocols.

Key responsibilities

• Coordinate daily study operations for assigned protocols, including tracking enrollment targets and key milestones
• Contact study participants to facilitate accurate and timely participation in research studies
• Maintain accurate study documentation and proactively monitor study progress, flagging risks to timelines or data quality

Required qualifications

• Educational exposure to clinical research methods and study design
• Experience with human subjects research and familiarity with informed consent and IRB requirements
• Strong time management and organizational skills, with the ability to prioritize across multiple studies
• Experience managing small projects or workstreams from start to finish
• High attention to detail and comfort working with structured data and documentation