Clinical Research Coordinator — Epilepsy Trials & Programs

George Washington University; Washington (District of Columbia); On-site; USD 45,000 - 70,000; Full time

Benefits offered by this job

Healthcare benefits

Tuition assistance

Well-being programs

Job summary

George Washington University in Foggy Bottom, Washington, DC, seeks a Clinical Research Operations Coordinator to support investigator-initiated and industry-sponsored trials, epilepsy surgery coordination, and academic program activities.

The role requires a BA/BS and 2 years of related experience, with familiarity with IRB submissions, GCP guidelines, and EDC systems preferred. Full-time, on-site, 40 hours/week with GW benefits. Salary range applies.

Qualifications

• BA/BS and 2 years of related experience required, degree must be conferred by start date.
• Certification preferred.
• Experience coordinating clinical trials in neurology, neuroscience, or academic medical center settings is desirable.

Responsibilities

• Coordinate day-to-day activities of investigator-initiated and industry-sponsored clinical trials.
• Assist with study start-up activities, including regulatory submissions, IRB documentation, study activation, and investigator files.
• Screen potential research participants and coordinate enrollment activities.
• Schedule research visits and ensure protocol adherence.
• Maintain study documentation in compliance with GCP, FDA, NIH, sponsor, and institutional requirements.
• Track recruitment, enrollment, study milestones, adverse events, and reporting deadlines.
• Coordinate communication among investigators, study sponsors, CROs, and research participants.
• Assist with preparation for monitoring visits and regulatory audits.

Skills

2 years experience

Regulatory knowledge

Data management

Excellent organizational skills

Education

BA/BS degree

Tools

REDCap

OnCore

Excel

Job description

George Washington University in Foggy Bottom, Washington, DC, seeks a Clinical Research Operations Coordinator to support investigator-initiated and industry-sponsored trials, epilepsy surgery coordination, and academic program activities.

The role requires a BA/BS and 2 years of related experience, with familiarity with IRB submissions, GCP guidelines, and EDC systems preferred. Full-time, on-site, 40 hours/week with GW benefits. Salary range applies.