Clinical Research Associate (CRA)

WE ARE HIRING | CLINICAL RESEARCH ASSOCIATE (CRA)📍 Location: Philippines🏠 Work Arrangement: Remote / Work From Home💼 Employment Type: Full-Time📅 Work Schedule: 5 Days per Week🌏 Main Office: Singapore

We are seeking a qualified and experienced Clinical Research Associate (CRA) based in the Philippines to support clinical research and clinical trial activities. The successful candidate will work remotely and collaborate closely with the Singapore-based Clinical Research and Operations Team, Principal Investigators, Study Coordinators, and clinical trial sites. Key Responsibilities

• Conduct remote and on-site monitoring visits for assigned clinical trial sites
• Conduct Site Qualification, Site Initiation, Interim Monitoring, and Close-Out Visits, as required
• Monitor clinical trial sites to ensure compliance with study protocols, ICH-GCP, and applicable regulations
• Review source documents, essential documents, informed consent documentation, and clinical trial data
• Identify, document, and follow up on protocol deviations, data queries, and site issues
• Ensure timely resolution of monitoring findings and action items
• Coordinate with Principal Investigators, Study Coordinators, and site research teams
• Monitor study progress, patient recruitment, enrollment, and site performance
• Prepare monitoring visit reports, follow-up letters, and other required documentation
• Maintain regular communication with the Singapore-based Clinical Research and Operations Team
• Support site management and other clinical research activities as assigned
• Travel when required for on-site monitoring and other study-related activities

Qualifications

• Bachelor's degree in Nursing, Pharmacy, Life Sciences, Medicine, Medical Technology, or a related field
• Minimum 2 years of experience in clinical research or clinical trials
• Previous CRA experience and clinical trial monitoring experience is preferred
• Experience conducting on-site and/or remote monitoring visits
• Good understanding of ICH-GCP and clinical trial regulations
• Strong organizational, analytical, documentation, and communication skills
• Proficient in English
• Ability to work independently and effectively in a remote environment
• Willingness to travel when required for site monitoring activities

What We Offer

• Full-time employment
• Work-from-home arrangement
• 5-day work week
• Opportunity to work with an international clinical research team
• Exposure to multinational clinical research projects and stakeholders