Senior Clinical Research Coordinator

Coordinates the implementation, quality control, and completion of research studies while assisting the Principal Investigator in determining and accomplishing study objectives. Oversees research studies in an administrative and operational capacity while maintaining compliance with guidelines set by governing agencies.

Responsibilities

• Coordinate day-to-day operations of clinical trials following GCP, study protocols, and regulations.
• Organize processes and study team activities to meet research objectives.
• Manage study visits, research procedures, and follow-up.
• Develop and maintain tracking tools and documentation; report study metrics to management.
• Support all stages of study visits: pre-study, qualification, initiation, monitoring, and close-out.
• Maintain source documentation and report adverse events.
• Recruit, screen, consent, and enroll participants.
• Collect and maintain patient and lab data.
• Act as liaison among participants, families, departments, external organizations, and government agencies.
• Work under direction of the Principal Investigator.

Requirements

• Bachelor’s degree (or equivalency) plus 8 years of directly related work experience, or Master’s degree (or equivalency) plus 6 years of directly related work experience.
• Education can substitute for experience on a 1:1 basis (e.g., 1 year of higher education = 1 year of directly related work experience).

Preferences

• Bachelor’s degree plus 8 years of directly related experience, or Master’s degree plus 6 years of directly related experience.

Pay

$68,000–$72,000 per year

Schedule

Full-time, Monday through Friday