Clinical Research Coordinator II

Job responsibilities

• Conduct study visits and procedures per protocol
• Maintain accurate source documentation and data entry
• Support regulatory compliance and visit readiness
• Coordinate with investigators, site staff, and senior study leads

Job requirements

• Experience supporting clinical trials in a site-based or physician practice setting
• Working knowledge of GCP, ICH, and site regulatory workflows
• Ability to manage multiple studies and competing priorities
• Strong attention to detail and documentation standards

Preferred qualifications

• Bachelor’s degree in life sciences, health sciences, or related field (or equivalent experience)
• 1–3 years of clinical research coordination experience
• Prior experience in a multi-study or fast-paced research environment

Core skills

• Source documentation and ALCOA+ principles
• Patient-facing communication and visit coordination
• Protocol interpretation and adherence
• EDC data entry and query resolution
• Time management across multiple studies

Why this version works

• Reads serious and professional, not templated
• Sets expectations without boxing you in
• Balances experience, education, and real-world capability
• Looks exactly like what sponsors and strong CRCs expect

‍