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

PPD (Thermo Fisher)

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, including remote or on-site visits to assess protocol and regulatory compliance

Job Summary

  • Perform and coordinate all aspects of the clinical monitoring and site management process, including remote or on-site visits to assess protocol and regulatory compliance.
  • Ensure that the trial is conducted in accordance with the approved protocol, ICH-GCP guidelines, applicable regulations, and SOPs to guarantee subjects' rights, well-being, and data reliability.
  • Offers a comprehensive Total Rewards package including medical and dental plans, paid time off, retirement programs, and stock purchase options.

Matching Summary

Perform and coordinate all aspects of the clinical monitoring and site management process, including remote or on-site visits to assess 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
  • Remote or on-site visits
  • 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

Cover Letter