Senior Clinical Research Associate (level dependent on experience)

📋 Description

• Oversee clinical site management activities across trials
• Ensure studies follow protocols, regulatory reqs, quality standards
• Serve as primary contact for assigned sites and investigators
• Conduct monitoring visits: pre-study, initiation, interim, close-out
• Support start-up activities: feasibility, site selection, regulatory docs
• Review and maintain trial master files and essential documents

🎯 Requirements

• Minimum 1 year clinical trial monitoring experience or equivalent
• Bachelor’s degree in healthcare-related field or equivalent
• RN qualification or equivalent clinical background considered
• Experience conducting studies in hospital/industry/CRO settings
• On-site monitoring experience preferred
• Strong knowledge of ICH-GCP, regulatory requirements, SOPs

🎁 Benefits

• Fully remote work opportunity
• Competitive compensation; sign-on bonus up to $10,000
• Comprehensive health benefits and vacation
• Paid parental leave and well-being programs
• Mentoring and leadership development
• Tuition reimbursement and ongoing training