Clinical Trial Associate
Clinical Trial Associate, APAC (Contract)
EPM Scientific are currently partnered with a growing Biotech in the Oncology space, which is actively . They are seeking a Clinical Trial Associate to join a growing Clinical Operations function supporting early- to late-phase studies. See a short summary below:
Contract Conditions:
- Start date: ASAP
- Location: Hybrid (3 days onsite in Jersey City / South San Francisco)
- Contract Type: Contract / Consultant - Full-time, 12-month initial duration
- Language: Fluency in one or more East Asian languages required (essential for site-facing activities)
- Project: Global Phase I-III Oncology Clinical Trials
Key Responsibilities:
- Support the planning, coordination, and operational delivery of global oncology clinical trials
- Assist with preparation, maintenance, and quality control of essential study documentation (protocols, consent forms, CRFs, study manuals)
- Support study start-up activities including site feasibility, site selection, and regulatory/ethics submissions
- Coordinate study-related meetings including investigator meetings and site initiation activities
- Support clinical data review activities, including query tracking and resolution within EDC systems
- Maintain Trial Master Files (TMFs) in collaboration with TMF support teams, ensuring inspection readiness
- Track trial progress metrics such as enrolment, timelines, and key milestones
- Support site monitoring activities in collaboration with monitoring and site engagement teams, as required
Requirements:
- Bachelor's degree with relevant clinical research experience or Advanced Degree with practical exposure to clinical trials
- Fluency in at least one Asian language (required for ongoing site communication)
- Previous experience in a Clinical Trials Associate, Study Coordinator, or similar clinical operations role
- Working knowledge of global clinical trial processes and regulatory requirements (ICH-GCP)
- Experience using CTMS and EDC platforms
If this role is of interest, please apply directly to learn more. If not, feel free to share with relevant contacts.
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