CRA (Level I)
Thermo Fisher Scientific · Bangkok, Thailand
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Role summary
Clinical Research Associate Level I at Thermo Fisher Scientific performing monitoring and site management for clinical trials in Bangkok. Responsible for conducting protocol compliance assessments, managing documentation, and ensuring data integrity across investigational sites using risk-based monitoring approaches.
What they're looking for
- Bachelor's degree in life sciences or related field
- Approximately 2 years of clinical monitoring or clinical research experience
- Strong knowledge of ICH-GCP guidelines and medical terminology
- Proficiency with Microsoft Office and clinical trial management systems
- Excellent written and oral communication skills in English
- Critical thinking and root cause analysis capabilities
- Valid driver's license where applicable
What you'll be doing
- Conduct remote and on-site monitoring visits using risk-based approaches to assess protocol and regulatory compliance
- Perform source data review, verification, and CRF audits to ensure data accuracy and completeness
- Document monitoring findings in reports and escalate deficiencies to clinical management for resolution
- Initiate trial sites, manage investigator payments, and coordinate close-out activities
- Maintain communication with investigational sites and ensure essential documents meet ICH-GCP requirements
Privacy & handoff
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