Clinical Research Associate (Client Dedicated)
IQVIA · Bangkok, Thailand
Clinical OperationsFull-timeCompany career page
The apply link worked recently (not employer-confirmed).
Role summary
Clinical Research Associate position focused on site monitoring and management for clinical studies in Bangkok. The role involves conducting monitoring visits, managing site communications, tracking study progress, and ensuring protocol compliance with GCP and ICH guidelines.
What they're looking for
- Bachelor's degree in scientific or healthcare discipline preferred
- Prior on-site clinical monitoring experience or equivalent education and training
- Knowledge of GCP and ICH regulatory guidelines
- Proficiency with Microsoft Office suite and computer systems
- Strong written and verbal English communication skills
- Organizational and problem-solving abilities
- Ability to manage relationships with sites, coworkers, and clients
What you'll be doing
- Conduct site monitoring visits including initiation, ongoing monitoring, and close-out activities per protocol and regulations
- Collaborate with sites on subject recruitment planning and track enrollment progress
- Provide protocol training to sites and maintain regular communication regarding study expectations
- Evaluate site compliance with protocol and regulations; escalate quality issues
- Track regulatory submissions, CRF completion, data queries, and recruitment metrics
Privacy & handoff
This role links to IQVIA's own application system. RoleLantern records your interest and checks the link, but the application happens on the employer's site and status updates may not come back to us. Clicking apply does not mark you as applied automatically.