Clinical Research Coordinator III

Job responsibilities

• Lead day-to-day execution of clinical trials within physician practices
• Oversee participant visits, source documentation, and protocol adherence
• Ensure data accuracy, completeness, and timely EDC entry
• Maintain visit readiness for monitoring, audits, and inspections
• Coordinate across multiple studies and therapeutic areas
• Serve as escalation point for complex protocol or operational issues
• Support training and oversight of junior coordinators as needed

Job requirements

• Experience coordinating clinical trials in a site-based or physician practice setting
• Strong working knowledge of GCP, ICH, and site regulatory workflows
• Ability to manage multiple studies and competing priorities independently
• Demonstrated attention to detail and documentation quality
• Comfortable collaborating with investigators, sponsors, and CRO partners

Preferred qualifications

• Bachelor’s degree in life sciences, health sciences, or related field (or equivalent experience)
• 3–5 years of clinical research coordination experience
• Prior experience supporting multiple concurrent studies
• Exposure to monitoring visits, queries, and audit readiness

Skills

• Advanced source documentation and ALCOA+ principles
• Protocol interpretation and operational execution
• EDC data entry, query resolution, and data review
• Patient-facing communication and visit coordination
• Time management across multiple studies and timelines

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