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