Sr. Clinical Research Associate, Iqvia

IQVIA

Base: $101,600.00 - $169,300.00; bonus/equity: dep...
2 years on-site monitoring experience
Good clinical practice (gcp) knowledge
Ich guidelines application skills
The role involves performing site monitoring visits including selection, initiation, monitoring, and close-out in accordance with Good Clinical Practice

Job Summary

  • The role involves performing site monitoring visits including selection, initiation, monitoring, and close-out in accordance with Good Clinical Practice.
  • Candidates will work with sites to adapt and drive subject recruitment plans to enhance predictability and project success.
  • The position requires ensuring the integrity of study site practices and maintaining accurate documentation in the Trial Master File.

Matching Summary

The role involves performing site monitoring visits including selection, initiation, monitoring, and close-out in accordance with Good Clinical Practice.

Salary

Base: $101,600.00 - $169,300.00; Bonus/Equity: Dependent on position; Benefits: Health, welfare, and other benefits offered

Skills & Requirements

Must-have

  • 2 years on-site monitoring experience
  • Good Clinical Practice (GCP) knowledge
  • ICH guidelines application skills

Nice-to-have

  • Oncology or cardiovascular therapeutic knowledge
  • Strong site communication abilities
  • Experience with regulatory submissions

Key Requirements

  • Bachelor's Degree in scientific discipline or health care preferred
  • At least 2 years of on-site monitoring experience
  • Knowledge of applicable clinical research regulatory requirements

Work Rights

Not specified

Tailored Resume

Cover Letter