Senior Clinical Research Associate

BeOne Medicines Ltd.

Base: $105,800.00 - $140,800.00 annually; bonus/eq...
Ich-gcp guidelines knowledge
Site monitoring experience
Protocol compliance assessment
The role involves managing and overseeing assigned clinical study sites to ensure data quality and patient safety in accordance with ICH-GCP guidelines

Job Summary

  • The role involves managing and overseeing assigned clinical study sites to ensure data quality and patient safety in accordance with ICH-GCP guidelines.
  • Candidates will collaborate with Clinical Study Teams to drive improvements in effectiveness and efficiencies within the Site Management group.
  • The company offers a comprehensive benefits package including medical, dental, vision, 401(k), and opportunities for equity awards.

Matching Summary

The role involves managing and overseeing assigned clinical study sites to ensure data quality and patient safety in accordance with ICH-GCP guidelines.

Salary

Base: $105,800.00 - $140,800.00 annually; Bonus/Equity: Eligible for annual bonus plan and discretionary equity awards; Benefits: Medical, Dental, Vision, 401(k), FSA/HSA, Life Insurance, Paid Time Off

Skills & Requirements

Must-have

  • ICH-GCP guidelines knowledge
  • site monitoring experience
  • protocol compliance assessment
  • SAE reconciliation skills
  • 4-6 years clinical operations

Nice-to-have

  • mentoring junior CRAs
  • global oncology trial experience
  • dashboard review capabilities
  • audit preparation support
  • collaborative spirit values

Key Requirements

  • BS/BA in scientific discipline
  • 3-4 years CRA monitoring experience
  • Minimum 4-6 years clinical operations experience

Work Rights

Not specified

Tailored Resume

Cover Letter