A leading clinical research company in Kuala Lumpur is seeking a Clinical Research Associate (CRA) to manage site monitoring and activities for clinical trials. Responsibilities include performing site visits, ensuring protocol compliance, and managing regulatory documents. Ideal candidates will possess a degree in Life Sciences, 2 years of CRA experience, and strong knowledge of ICH-GCP. This position requires fluency in English and familiarity with eClinical systems. Candidates will work in a collaborative environment ensuring compliance with local regulations.
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