Contract Senior Cra

ICON

Home-based anywhere in the U.S.
Competitive salary; not specified; benefits includ...
**
Minimum 3 years independent monitoring experience
Valid driver's license required
Ability to travel at least 60% of time
** ICON is seeking a Contract Senior Clinical Research Associate for a fully remote position in the U.S. This role involves conducting clinical trial monitoring, ensuring compliance, and collaborating with research teams, requiring relevant experience and strong organizational skills. **

Job Summary

  • ICON is a world-leading healthcare intelligence and clinical research organization seeking a Contractor Senior Clinical Research Associate for a 6-month contract.
  • The role involves conducting site qualification, initiation, monitoring, and close-out visits while ensuring protocol compliance and patient safety throughout the trial process.
  • ICON offers competitive benefits including various annual leave entitlements, health insurance offerings, retirement planning, and a global Employee Assistance Programme.

Matching Summary

Match Score: 75

** ICON is seeking a Contract Senior Clinical Research Associate for a fully remote position in the U.S. This role involves conducting clinical trial monitoring, ensuring compliance, and collaborating with research teams, requiring relevant experience and strong organizational skills. **

Salary

Competitive salary; Not specified; Benefits include health insurance, retirement planning, and global assistance programs

Skills & Requirements

Must-have

  • Minimum 3 years independent monitoring experience
  • Valid driver's license required
  • Ability to travel at least 60% of time
  • Bachelor's degree in scientific or health-related field
  • In-depth knowledge of ICH-GCP guidelines

Nice-to-have

  • Strong organizational and communication skills
  • Experience in study coordinator or nursing role
  • Ability to work independently in fast-paced environment
  • Collaborative team player with attention to detail

Key Requirements

  • 3 years independent monitoring experience
  • Bachelor's degree in science or health field
  • Valid driver's license
  • Knowledge of clinical trial regulations and ICH-GCP
  • US work authorization (implied by location)

Work Rights

Not specified

Tailored Resume

Cover Letter