Senior Clinical Research Associate

BeOne Medicines

Base: $105,800.00 - $140,800.00 annually; bonus/eq...
Ich-gcp guidelines knowledge
3-4 years cra monitoring experience
Site visit coordination and documentation
The role involves managing and overseeing clinical study sites to ensure data quality and patient safety in accordance with ICH-GCP guidelines

Job Summary

  • The role involves managing and overseeing clinical study sites to ensure data quality and patient safety in accordance with ICH-GCP guidelines.
  • Candidates will mentor junior Clinical Research Associates and collaborate with Clinical Study Teams to optimize effectiveness and efficiencies.
  • The company offers a comprehensive benefits package including medical, dental, vision, 401(k), and opportunities for discretionary equity awards.

Matching Summary

The role involves managing and overseeing 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
  • 3-4 years CRA monitoring experience
  • Site visit coordination and documentation
  • SAE reconciliation and resolution
  • Data collection and tracking

Nice-to-have

  • Mentoring less experienced CRAs
  • Global oncology trial experience
  • Proactive improvement initiatives
  • Collaborative spirit with teams
  • Dashboard review and risk assessment

Key Requirements

  • BS/BA in scientific discipline
  • 4-6 years Clinical Operations experience
  • 3-4 years CRA monitoring experience
  • Knowledge of ICH regulatory guidelines

Work Rights

Not specified

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