Sr. Cra, Sponsor Aligned, Oncology

IQVIA UK

Multiple Locations, United Kingdom
Base: $57,500.00 - $226,800.00; bonus/equity: ince...
Gcp and ich guidelines
Phase 1 oncology trials
Site monitoring visits
You’ll play a pivotal role in monitoring and managing clinical trial sites to ensure compliance with study protocols, regulations, and sponsor requirements

Job Summary

  • You’ll play a pivotal role in monitoring and managing clinical trial sites to ensure compliance with study protocols, regulations, and sponsor requirements.
  • Be at the forefront of groundbreaking cancer research and make a real impact on patients’ lives.
  • You’ll have the opportunity to work on cutting-edge Phase 1 oncology trials, collaborate with top professionals in the field, and contribute to life-changing advancements in cancer treatment.

Matching Summary

You’ll play a pivotal role in monitoring and managing clinical trial sites to ensure compliance with study protocols, regulations, and sponsor requirements.

Salary

Base: $57,500.00 - $226,800.00; Bonus/Equity: Incentive plans, bonuses may be offered; Benefits: Range of health and welfare and/or other benefits

Skills & Requirements

Must-have

  • GCP and ICH guidelines
  • Phase 1 oncology trials
  • Site monitoring visits
  • Subject recruitment plans
  • Trial Master File (TMF)

Nice-to-have

  • Collaboration with study team
  • Mentorship of clinical staff
  • Cutting-edge research opportunities

Key Requirements

  • 3+ years oncology monitoring experience
  • 1.5+ years oncology monitoring experience
  • Phase 1 oncology experience required
  • BS degree required
  • Scientific or healthcare degree preferred

Work Rights

Not specified

Tailored Resume

Cover Letter