Senior / Clinical Research Associate
IQVIA · Wilayah Persekutuan Kuala Lumpur, Malaysia
Clinical OperationsFull-timeCompany career page
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Role summary
IQVIA seeks a Senior Clinical Research Associate or CRA to conduct site visits, manage study progress, and ensure regulatory compliance for clinical trials. The role offers career development in clinical operations with exposure to global projects and mentorship support.
What they're looking for
- University degree in scientific or healthcare discipline
- Minimum 1 year on-site monitoring experience in clinical research
- Strong knowledge of GCP and clinical research regulatory requirements
- Proficient with MS Office and general computer applications
- Fluent English communication skills
- Strong organizational, time management, and problem-solving abilities
- Willingness to travel for site visits
What you'll be doing
- Conduct site selection, initiation, monitoring, and close-out visits with proper documentation
- Support development of subject recruitment strategies and monitor enrollment progress
- Establish communication protocols and deliver protocol training to assigned research sites
- Assess site compliance and data quality, escalating integrity issues as needed
- Track regulatory submissions, case report form completion, and resolve data queries
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.