Regional Clinical Trial Operations Lead

BeiGene Ltd.

United States

Remote

USD 73,000 - 98,000

Full time

4 days ago
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Benefits offered by this job

Medical insurance
Dental insurance
Vision insurance
401(k)
FSA/HSA
Life insurance
Paid time off
Wellness program

Job summary

BeOne Medicines Ltd. is seeking an experienced Regional Trial Support professional in the United States. The role supports the Regional Clinical Study Manager in regional study delivery, collaborates with CRAs, SSUSs, and global teams, and helps maintain study documentation across CTMS/eTMF systems.

The candidate should have a scientific or healthcare background and 1+ years of clinical research experience, with strong organizational and communication skills for cross-functional collaboration.

Qualifications

  • Bachelor’s degree in a scientific or healthcare discipline is preferred.
  • Minimum 1 year of clinical research experience in biotech, pharma or CRO.
  • Knowledge of clinical operations methodologies and regulatory requirements.

Responsibilities

  • Supports Regional Clinical Study Manager in regional study delivery within timelines and budget.
  • Coordinates with CRAs and SSUSs on CTMS updates, document collection and ISF binder prep.
  • Assists in country study delivery and TMF creation/maintenance at country level.
  • Collaborates with regional stakeholders and supports investigator meetings and regional team activities.
  • Might support monitoring visit prep, regulatory submissions, and TMF quality checks.

Skills

MS Office
eTMF
CTMS

Education

Bachelor’s degree in science/healthcare
Advanced degree preferred

Tools

CTMS
eTMF

Job description

BeOne Medicines Ltd. is seeking an experienced Regional Trial Support professional in the United States. The role supports the Regional Clinical Study Manager in regional study delivery, collaborates with CRAs, SSUSs, and global teams, and helps maintain study documentation across CTMS/eTMF systems.

The candidate should have a scientific or healthcare background and 1+ years of clinical research experience, with strong organizational and communication skills for cross-functional collaboration.

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