Principal Clinical Research Associate

Responsibilities

• Serve as Lead CRA for complex clinical studies, overseeing site activities and compliance
• Participate in site feasibility assessments and site selection processes
• Ensure study conduct aligns with protocols and regulatory requirements
• Prioritize patient safety and oversee informed consent processes
• Review and report adverse events and protocol deviations
• Maintain accurate and audit-ready regulatory documentation
• Identify and manage study risks to ensure compliance

Qualifications

• Bachelor’s degree or higher in a healthcare or science-related field
• Minimum of five years of field-based CRA experience in the medical device and/or pharmaceutical industry
• Experience across multiple phases of clinical research and product development
• Experience with IVD and/or POC studies strongly preferred
• Laboratory experience in molecular biology, microbiology, or blood culture is highly desirable
• Proficiency with Veeva Vault CTMS and CDMS required
• Strong understanding of clinical trial operations and data management

Benefits

• Comprehensive Total Rewards program supporting employee development
• Performance-based recognition and rewards
• Competitive package of compensation and benefits programs

Pay

• $117,800 – $188,600 annually

Schedule

• Remote - US based candidates only, no visa sponsorship available