Bangkok, Thailand
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Listing record updated: November 1, 2026. We archive records after 60 days without an update. This date does not confirm that the employer is still hiring.
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The CRA (Level I) at Thermo Fisher Scientific performs and coordinates clinical monitoring and site management for clinical trials conducted in Bangkok, Thailand. Responsibilities include conducting remote and on-site monitoring visits, assessing protocol and regulatory compliance, reviewing data accuracy, managing investigational product inventory, documenting observations, and maintaining communication with investigational sites. The role requires a bachelor's degree in a life sciences field and approximately 2 years of relevant clinical monitoring experience, along with knowledge of ICH-GCP, applicable regulations, and risk-based monitoring concepts. Travel is required extensively, generally 60–80% or higher.
Monitor investigator sites using a risk-based monitoring approach, applying root cause analysis and problem-solving
Ensure data accuracy through SDR, SDV, and CRF review via on-site and remote monitoring
Document monitoring observations in reports and letters, escalating deficiencies to clinical management
Initiate clinical trial sites and perform trial close-out activities, ensuring ICH-GCP compliance
Maintain CTMS and trial status tracking, and facilitate communication among sites, clients, and project teams
Bachelor's degree in a life sciences-related field
Approximately 2 years of clinical monitoring or related experience
Basic medical/therapeutic-area knowledge and understanding of medical terminology
Working knowledge of ICH-GCP and applicable regulations
Good English language, communication, organizational, and computer skills
Experience with FSO, FSP, and Government monitoring environments; valid driver's license where applicable
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