Sr. Cra, Sponsor Aligned, Oncology

IQVIA UK

Base: $71,900.00 - $189,000.00 annualized; bonus/e...
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3+ years on-site oncology monitoring experience
Phase 1 oncology trial experience required
Proficiency in gcp and ich guidelines
** IQVIA UK is seeking a Senior Clinical Research Associate specializing in oncology to monitor and manage clinical trial sites, ensuring compliance with study protocols and regulatory guidelines. The ideal candidate should have at least 3 years of oncology monitoring experience, particularly in Phase 1 trials, and possess strong communication and organizational skills. **

Job Summary

  • You will play a pivotal role in monitoring and managing clinical trial sites to ensure compliance with study protocols and regulations.
  • The position requires conducting selection, initiation, monitoring, and close-out visits while ensuring robust subject recruitment plans are met.
  • This role offers the opportunity to work on cutting-edge Phase 1 oncology trials contributing to life-changing advancements in cancer treatment.

Matching Summary

Match Score: 75

** IQVIA UK is seeking a Senior Clinical Research Associate specializing in oncology to monitor and manage clinical trial sites, ensuring compliance with study protocols and regulatory guidelines. The ideal candidate should have at least 3 years of oncology monitoring experience, particularly in Phase 1 trials, and possess strong communication and organizational skills. **

Salary

Base: $71,900.00 - $189,000.00 annualized; Bonus/Equity: Incentive plans and bonuses may be offered; Benefits: Health, welfare, and other benefits included

Skills & Requirements

Must-have

  • 3+ years on-site oncology monitoring experience
  • Phase 1 oncology trial experience required
  • Proficiency in GCP and ICH guidelines

Nice-to-have

  • Strong therapeutic knowledge in oncology
  • Mentorship of clinical staff
  • Effective communication skills

Key Requirements

  • BS degree in scientific discipline or healthcare
  • Minimum 3 years on-site oncology monitoring experience
  • Required Phase 1 oncology experience

Work Rights

Not specified

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