Clinical Research Coordinator

Responsibilities

• Coordinate day-to-day study activities, including study startup, participant scheduling, and monitoring visits.
• Collaborate with investigators, research nurses, and sponsors to ensure accurate execution of protocol procedures.
• Conduct participant screening, eligibility verification, and the informed consent process.
• Support clinical procedures such as vital sign collection, dermatologic assessments, and sample processing.
• Maintain accurate source documentation and complete electronic data capture entries.
• Ensure compliance with federal regulations, Good Clinical Practice (GCP), and institutional policies.
• Organize and maintain essential regulatory and study documentation for audits and inspections.

Requirements

• Bachelor’s degree with 1 year of experience in clinical research OR experience in a clinical environment with direct interaction with patients and healthcare staff.
• Excellent oral and written communication skills.
• Strong organizational skills and high level of attention to detail.
• Ability to work independently and manage competing deadlines.

Preferred Qualifications

• Experience in dermatology research or other outpatient specialty research settings.
• Knowledge of clinical research regulatory requirements (FDA, ICH-GCP, OHRP, IRB).
• Experience supporting sponsor-initiated or investigator-initiated trials in an academic setting.
• Familiarity with clinical billing practices and workflow coordination.
• Experience with electronic data capture systems and electronic medical records.

About the Company

Wright State University is an equal opportunity employer dedicated to advancing research and education. The Pharmacology Translational Unit (PTU) conducts vital clinical and translational research studies to improve healthcare outcomes.