Global Clinical Trials Operations Associate

BeiGene, Ltd.

United States

Remote

USD 73,000 - 98,000

Full time

2 days ago
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Benefits offered by this job

Medical benefits
Dental benefits
Vision benefits
401(k)
FSA/HSA
Life Insurance
Paid Time Off
Wellness program

Job summary

BeOne Medicines Ltd. in the United States is seeking an experienced professional to support the Global Clinical Study Manager in delivering clinical studies with quality and on time.

You will help organize CST meetings, manage study systems (eTMF, CTMS, SharePoint) and coordinate study plans, with responsibilities across cross-functional teams. Bachelor or higher in science/healthcare; 1+ year in clinical research; limited travel; comprehensive benefits.

Qualifications

  • Bachelor or higher in a scientific or healthcare discipline (higher degree preferred).
  • 1+ years of clinical research experience in biotech, pharma, or CRO.
  • Knowledge of clinical operations methodologies and regulatory guidelines (ICH-GCP).

Responsibilities

  • Supports the Global Clinical Study Manager with organization and logistics for cross-functional CST meetings.
  • Sets up the study in systems such as eTMF and CTMS; maintains up-to-date study-level information.
  • Ensures system access and user management across the study lifecycle; supports development of study plans.
  • Ensures timely preparation of study newsletters and other correspondence related to study conduct.
  • Supports TMF specialist with study-level TMF creation and QC per the TMF plan.

Skills

MS Office Suite
Clinical operations knowledge
Clinical research experience

Education

Bachelor's degree or higher in science/healthcare

Tools

eTMF
CTMS
SharePoint

Job description

BeOne Medicines Ltd. in the United States is seeking an experienced professional to support the Global Clinical Study Manager in delivering clinical studies with quality and on time.

You will help organize CST meetings, manage study systems (eTMF, CTMS, SharePoint) and coordinate study plans, with responsibilities across cross-functional teams. Bachelor or higher in science/healthcare; 1+ year in clinical research; limited travel; comprehensive benefits.

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