Oncology Clinical Trials Associate, APAC (Contract)

Eikon Therapeutics

Jersey City, Millbrae (NJ, CA)

On-site

USD 69,000 - 83,000

Full time

8 days ago

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Job summary

Eikon Therapeutics is seeking a Clinical Trial Associate, APAC (Contract) in Jersey City, NJ or Millbrae, CA. You will support planning, coordination, and execution of Phase I-III insourced global oncology studies, collaborating with cross-functional teams to drive trial success.

The role requires bilingual fluency in English and Mandarin/Cantonese/Japanese/Korean, with on-site presence and strong experience in CTMS/EDC systems. Equal opportunity employer and dynamic growth opportunities.

Qualifications

  • Advanced degree or Bachelor’s with 2 years in a relevant field (life sciences, healthcare, or related).
  • Ability to communicate in multiple languages is required.
  • Experience as a Clinical Trials Associate, Study Coordinator, or similar role in pharma/biotech/CRO preferred.

Responsibilities

  • Prepare and maintain study documents (protocols, ICFs, CRFs, and related materials).
  • Coordinate site startup activities: site selection, feasibility, ethics submissions.
  • Organize investigator meetings and study initiation visits.
  • Track distribution and reconciliation of trial supplies and investigational products.
  • Review data queries and ensure data accuracy in EDC systems.
  • Maintain TMFs and trial documentation per regulatory requirements.
  • Facilitate communication among study team, investigators and sites.
  • Monitor patient recruitment and study progress to meet timelines.
  • Assist with site monitoring visits and ensure adherence to monitoring plans.
  • Stay updated on oncology clinical trial regulations and best practices.

Skills

English
Multilingual

Education

Advanced Degree or Bachelor's with 2 years in life sciences

Tools

CTMS
EDC systems
Microsoft Office

Job description

Eikon Therapeutics is seeking a Clinical Trial Associate, APAC (Contract) in Jersey City, NJ or Millbrae, CA. You will support planning, coordination, and execution of Phase I-III insourced global oncology studies, collaborating with cross-functional teams to drive trial success.

The role requires bilingual fluency in English and Mandarin/Cantonese/Japanese/Korean, with on-site presence and strong experience in CTMS/EDC systems. Equal opportunity employer and dynamic growth opportunities.

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