Senior/Clinical Research Associate (Client Dedicated)

IQVIA · Ho Chi Minh, Vietnam

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Clinical OperationsFull-timeCompany career page

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Role summary

IQVIA seeks a Senior or Clinical Research Associate for a client-dedicated role in Ho Chi Minh, Vietnam. The position involves site management, regulatory compliance oversight, and coordination of clinical trial activities, with opportunities for career advancement into operations and project management.

What they're looking for

University degree in scientific discipline or healthcare field
Minimum 1 year of on-site clinical trial monitoring experience
Strong knowledge of GCP and clinical research regulatory requirements
Proficient with MS Office and standard computer applications
Fluent English language skills, spoken and written
Strong organizational, time management, and problem-solving abilities
Willingness to travel as required for site visits

What you'll be doing

Conduct site selection, initiation, monitoring, and close-out visits with appropriate documentation
Support development and implementation of subject recruitment strategies
Establish communication protocols and deliver protocol training to assigned research sites
Assess and ensure quality and integrity of site practices, escalating issues as needed
Track trial progress including regulatory submissions, enrollment, CRF completion, and data queries

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