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Clinical Trial Associate

EPM Scientific
Jersey, NJ Contractor
POSTED ON 4/16/2026
AVAILABLE BEFORE 5/16/2026

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.

Hourly Wage Estimation for Clinical Trial Associate in Jersey, NJ
$48.00 to $61.00
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