Site Management Associate II
ICON · Kuala Lumpur, Malaysia
Clinical OperationsFull-timeCompany career page
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Role summary
Site Management Associate II role supporting clinical trial operations at a global contract research organization. The position involves coordinating monitoring activities, ensuring regulatory compliance, and managing site performance across study lifecycles in a sponsor-dedicated model.
What they're looking for
- Bachelor's degree in life sciences, healthcare administration, or clinical research
- Clinical research, site management, or monitoring experience with GCP knowledge
- Strong organizational and project management abilities with multitasking capacity
- Analytical skills with meticulous attention to detail and quality focus
- Excellent communication and relationship-building skills with diverse stakeholders
- Willingness to travel approximately 25% as required
- Legal right to work in Malaysia
What you'll be doing
- Coordinate site monitoring activities ensuring protocol adherence and timely issue resolution
- Prepare and review regulatory documents for GCP and regulatory compliance
- Collaborate across teams to facilitate communication and support throughout trial lifecycle
- Track and analyze site performance metrics, generating efficiency reports
- Participate in training initiatives and mentor junior clinical trial management staff
Privacy & handoff
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