Clinical Research Coordinator II: Own Your Studies

Lever, Inc.; Carlsbad (CA); Hybrid; USD 65,000 - 90,000; Full time

Benefits offered by this job

Health Insurance

Paid Time Off

Retirement Plan

Professional Development

Job summary

Profound Research seeks a Clinical Research Coordinator II to manage assigned studies on-site, from start-up through closeout, coordinating patient visits and interactions while ensuring audit-ready documentation and regulatory compliance. You will work directly with investigators, sponsors, and CROs to uphold patient safety and data integrity.

The role emphasizes ownership of study activities, independent execution, and proactive communication.

Qualifications

• Bachelor’s degree with 1+ year of relevant experience, OR Associate’s degree with 3+ years of relevant experience, OR High school diploma with 4+ years of relevant experience and at least 1 year of CRC experience
• Experience performing clinical procedures including vital signs, EKGs, phlebotomy, and lab processing
• Comfortable working independently and managing competing priorities
• Strong documentation skills and familiarity with EDC platforms and clinical trial management systems

Responsibilities

• Serve as primary coordinator for assigned clinical trials, managing study activities from start-up through closeout
• Execute full visit flow independently – participant visits, protocol procedures, data collection, and documentation
• Lead patient interactions with clarity and compassion, ensuring participants feel informed and supported throughout their study experience
• Maintain accurate, timely, audit-ready documentation across source documents, CRFs, and EDC systems
• Track and report adverse events, deviations, and safety findings in accordance with protocol and regulatory requirements
• Communicate directly and professionally with investigators, sponsors, CROs, and internal teams
• Support site readiness for monitoring visits and audits

Skills

Clinical procedures

Documentation skills

EDC platforms familiarity

Education

Bachelor or higher / CRC experience

Tools

EDC systems

Job description

Profound Research seeks a Clinical Research Coordinator II to manage assigned studies on-site, from start-up through closeout, coordinating patient visits and interactions while ensuring audit-ready documentation and regulatory compliance. You will work directly with investigators, sponsors, and CROs to uphold patient safety and data integrity.

The role emphasizes ownership of study activities, independent execution, and proactive communication.