Sr. Sma (safety Activities)

ICON Clinical Research, LP

Mexico City, Mexico
Fully remote
Site management activities
Clinical trial protocols
Regulatory requirements
As a Senior Site Management Associate at ICON, you will play a critical role in overseeing site management activities, ensuring the smooth operation of clinical trials at the site level

Job Summary

  • As a Senior Site Management Associate at ICON, you will play a critical role in overseeing site management activities, ensuring the smooth operation of clinical trials at the site level.
  • You will work closely with clinical teams, providing guidance and support to ensure that sites meet regulatory and operational requirements while delivering high-quality data and achieving study goals.
  • ICON offers a range of additional benefits designed to be competitive within each country and focused on well-being and work life balance opportunities for you and your family.

Matching Summary

As a Senior Site Management Associate at ICON, you will play a critical role in overseeing site management activities, ensuring the smooth operation of clinical trials at the site level.

Skills & Requirements

Must-have

  • site management activities
  • clinical trial protocols
  • regulatory requirements
  • GCP
  • data collection and reporting

Nice-to-have

  • fostering collaboration
  • process improvement
  • strong site relationships
  • inclusive environment
  • nurtures talent

Key Requirements

  • Bachelor’s degree in life sciences
  • Extensive experience in site management
  • Strong understanding of clinical trial processes
  • Excellent problem-solving skills
  • Effective communication skills

Work Rights

Not specified

Tailored Resume

Cover Letter