CRA II

ICON · Kuala Lumpur, Malaysia

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Clinical OperationsFull-timeCompany career page

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Role summary

Clinical Research Associate II position supporting clinical trial monitoring activities. Responsibilities include site visits, protocol compliance oversight, data quality management, and documentation review. Based in Kuala Lumpur, Malaysia.

What they're looking for

Bachelor's degree in scientific or healthcare-related field
Minimum 2 years of Clinical Research Associate experience
In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines
Strong organizational and communication skills with attention to detail
Ability to work independently and collaboratively in fast-paced environment
Willingness to travel approximately 60% as required
Legal right to work in Malaysia

What you'll be doing

Conduct site qualification, initiation, monitoring, and close-out visits for clinical trials
Ensure protocol compliance, data integrity, and patient safety throughout trial process
Collaborate with investigators and site staff to facilitate smooth study conduct
Review data and resolve queries to maintain high-quality clinical data
Prepare and review study documentation including protocols and clinical study reports

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Date posted5 days ago

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