Clinical Trial Assistant

ICON

Multiple Locations
Clinical trial coordination and administration
Clinical trial documentation management
Regulatory compliance in clinical trials
As a Clinical Trial Assitant at ICON, you will play a pivotal role in assisting with the design and analysis of clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies

Job Summary

  • As a Clinical Trial Assitant at ICON, you will play a pivotal role in assisting with the design and analysis of clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies.
  • ICON offers a range of benefits including various annual leave entitlements, health insurance options, competitive retirement planning, and a Global Employee Assistance Programme to support well-being.
  • ICON is dedicated to providing an inclusive and accessible environment for all candidates and is committed to a workplace free of discrimination and harassment.

Matching Summary

As a Clinical Trial Assitant at ICON, you will play a pivotal role in assisting with the design and analysis of clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies.

Skills & Requirements

Must-have

  • clinical trial coordination and administration
  • clinical trial documentation management
  • regulatory compliance in clinical trials
  • cross-functional team collaboration
  • clinical trial metrics tracking

Nice-to-have

  • excellent organizational skills
  • strong communication skills
  • ability to work in fast-paced environment
  • attention to detail
  • inclusive and diverse culture

Key Requirements

  • Bachelor's degree in scientific or healthcare-related field
  • prior experience or strong interest in clinical research
  • knowledge of clinical trial processes and regulations

Work Rights

Not specified

Tailored Resume

Cover Letter