Senior Clinical Research Associate

BeiGene

Remote
$105,800.00 - $140,800.00 annually; bonus/equity: ...
Ich-gcp guidelines
Site monitoring
Data quality
The SCRA is primarily a site monitor and is responsible for the management and oversight of their assigned clinical study sites to ensure data quality and patient safety in accordance with ICH-GCP guidelines, local regulations, and applicable SOPs

Job Summary

  • The SCRA is primarily a site monitor and is responsible for the management and oversight of their assigned clinical study sites to ensure data quality and patient safety in accordance with ICH-GCP guidelines, local regulations, and applicable SOPs.
  • Proactively seeks opportunities to lead and drive improvements to optimize effectiveness and efficiencies within the Site Management group as well as within the greater Americas region.
  • The Company has a comprehensive benefits package that includes Medical, Dental, Vision, 401(k), FSA/HSA, Life Insurance, Paid Time Off, and Wellness.

Matching Summary

The SCRA is primarily a site monitor and is responsible for the management and oversight of their assigned clinical study sites to ensure data quality and patient safety in accordance with ICH-GCP guidelines, local regulations, and applicable SOPs.

Salary

$105,800.00 - $140,800.00 annually; Bonus/Equity: Annual bonus plan, discretionary equity awards, Employee Stock Purchase Plan; Benefits: Medical, Dental, Vision, 401(k), FSA/HSA, Life Insurance, Paid Time Off, Wellness

Skills & Requirements

Must-have

  • ICH-GCP guidelines
  • site monitoring
  • data quality
  • patient safety
  • clinical study teams

Nice-to-have

  • fighting cancer
  • collaborative spirit
  • entrepreneurial mindset
  • continuous learning

Key Requirements

  • 4-6 years relevant Clinical Operations experience
  • 3-4 years CRA monitoring experience
  • BS/BA scientific discipline
  • Global oncology trials experience preferred

Work Rights

Not specified

Tailored Resume

Cover Letter