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Clinical Research Associate II responsible for monitoring clinical trials remotely from Malaysia, maintaining protocol compliance, data quality, and participant safety across study sites for ICON.
विवरण
- Manage site qualification, initiation, monitoring, and close-out visits for clinical trials.
- Maintain compliance with study protocols, data integrity standards, and patient-safety requirements.
- Coordinate with investigators and site teams to support effective study execution.
- Review clinical data and resolve queries to uphold data quality.
- Help prepare and review study materials, including protocols and clinical study reports.
- Support a sponsor-dedicated engagement backed by ICON’s global clinical research expertise.
आवश्यकताएँ
- Bachelor’s degree in a scientific or healthcare-related discipline.
- At least two years of experience working as a Clinical Research Associate.
- Detailed understanding of clinical trial operations, applicable regulations, and ICH-GCP guidelines.
- Strong organizational and communication abilities, with consistent attention to detail.
- Capacity to work independently and collaborate effectively in a fast-paced setting.
- Availability to travel as needed, approximately 60% of the time.
- Legal authorization to work in Malaysia.
लाभ
- Competitive base pay with performance-related incentives.
- Health and wellbeing programmes, including medical, dental, and vision coverage where applicable.
- Retirement and pension plan options.
- Life assurance and disability coverage.
- Employee assistance programmes and wellbeing resources.
- Structured training, learning resources, and career development pathways.
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