Site Specialist I

ICON

Multiple Locations
Clinical trial site management
Protocol compliance assurance
Data integrity maintenance
ICON plc is a world-leading healthcare intelligence and clinical research organization fostering an inclusive environment driving innovation and excellence

Job Summary

  • ICON plc is a world-leading healthcare intelligence and clinical research organization fostering an inclusive environment driving innovation and excellence.
  • As a Site Specialist at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to innovative treatments and therapies.
  • ICON offers competitive salary and a range of benefits focused on well-being and work-life balance, including health insurance, retirement planning, and global employee assistance programs.

Matching Summary

ICON plc is a world-leading healthcare intelligence and clinical research organization fostering an inclusive environment driving innovation and excellence.

Skills & Requirements

Must-have

  • Clinical trial site management
  • Protocol compliance assurance
  • Data integrity maintenance
  • Patient safety monitoring
  • Collaboration with investigators
  • Clinical data review

Nice-to-have

  • Strong organizational skills
  • Effective communication skills
  • Ability to work independently
  • Team collaboration in fast-paced environment
  • Attention to detail

Key Requirements

  • Bachelor's degree in scientific or healthcare field
  • Minimum 3 years experience as SSU
  • Knowledge of clinical trial processes and ICH-GCP guidelines

Work Rights

Not specified

Tailored Resume

Cover Letter