Clinical Research Associate (level Ii) - Fsp Oncology- Northeastus

Thermo Fisher Scientific UK

New York, United States
Base: $100,000.00–$140,000.00; bonus/equity: varia...
On-site
Risk-based monitoring approach
Ich-gcp guidelines
Site processes specialist
Perform and coordinate all aspects of the clinical monitoring and site management process, ensuring protocol and regulatory compliance

Job Summary

  • Perform and coordinate all aspects of the clinical monitoring and site management process, ensuring protocol and regulatory compliance.
  • Conduct remote or on-site visits, assess investigational product, and document observations in timely reports.
  • The company offers a comprehensive Total Rewards package including medical, dental, vision plans, paid time off, and retirement savings programs.

Matching Summary

Perform and coordinate all aspects of the clinical monitoring and site management process, ensuring protocol and regulatory compliance.

Salary

Base: $100,000.00–$140,000.00; Bonus/Equity: Variable annual bonus based on performance; Benefits: Comprehensive Total Rewards package

Skills & Requirements

Must-have

  • Risk-based monitoring approach
  • ICH-GCP guidelines
  • Site processes specialist
  • Data accuracy through SDR, SDV
  • Investigational product assessment

Nice-to-have

  • Root cause analysis
  • Critical thinking and problem-solving
  • Collaborative relationships with sites
  • Effective communication skills

Key Requirements

  • Bachelor's degree in life sciences or equivalent
  • 1 year clinical research monitor experience
  • Valid driver's license

Work Rights

Not specified

Tailored Resume

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