Sr Clinical Research Associate

📋 Description

• Conduct remote and on-site monitoring per protocols and plans
• Ensure sites remain compliant with regulations and sponsor requirements
• Manage site activities including initiation, monitoring, and closeout
• Maintain CTMS data and monitor EDC data entry; support eCRF queries
• Mentor junior CRAs and train project teams
• Travel extensively across North America up to 80%

🎯 Requirements

• Bachelor’s degree in Life Sciences or equivalent experience
• At least 36 months on-site clinical monitoring experience
• Strong knowledge of medical terminology, regulatory requirements, and trial guidelines
• Experience with CTMS, eTMF, EDC, and MS Office
• Excellent communication, problem-solving, and documentation skills
• Willingness to travel up to 80% across North America

🎁 Benefits

• Remote work opportunities
• Competitive salary
• 401(k) retirement plan with company match
• Tuition reimbursement
• Flexible work environment
• Discretionary PTO and paid holidays