Clinical Trial Associate, APAC

Role: Clinical Trials Associate, APAC in Oncology, supporting planning, coordination, and execution of Phase I-III global clinical studies. Responsibilities include preparing study documents, managing site activities, coordinating trial supplies, reviewing data queries, maintaining trial master files, and ensuring regulatory compliance. The role requires facilitating communication among study teams and tracking trial progress, with a focus on oncology indications across early to late-phase trials. Requirements: Bachelor's degree with 2+ years relevant experience, fluency in Mandarin, Cantonese, Japanese, or Korean, knowledge of ICH-GCP and FDA regulations, proficiency in CTMS and EDC systems, strong organizational and communication skills. Preferred: prior experience in clinical operations within biotech or pharma, familiarity with oncology clinical trials. HighValue: oncology (early to late-phase), multi-language capability for Asia, global trial coordination, regulatory compliance, knowledge of GxP standards, and experience with clinical trial systems. WorkSetup: hybrid onsite in Jersey City or Millbrae, with at least 3 days per week onsite.