Group Lead, Clinical Trial Associate

ICON Clinical Research, LP

Not specified; competitive salary offered; various...
Clinical trial administration experience
Team leadership and management skills
Regulatory compliance knowledge
The role involves supervising a team to ensure timely and accurate processing of essential trial documents including regulatory submissions and study contracts

Job Summary

  • The role involves supervising a team to ensure timely and accurate processing of essential trial documents including regulatory submissions and study contracts.
  • Candidates must implement and monitor standard operating procedures to maintain strict compliance with regulatory guidelines and internal quality standards.
  • ICON offers competitive benefits including health insurance, retirement planning, and a global employee assistance program focused on well-being.

Matching Summary

The role involves supervising a team to ensure timely and accurate processing of essential trial documents including regulatory submissions and study contracts.

Salary

Not specified; Competitive salary offered; Various annual leave entitlements and health insurance included

Skills & Requirements

Must-have

  • Clinical trial administration experience
  • Team leadership and management skills
  • Regulatory compliance knowledge
  • SOP implementation and monitoring
  • Cross-functional collaboration abilities

Nice-to-have

  • Bachelor's degree in life sciences
  • Advanced degree preferred
  • Continuous improvement culture
  • Professional development mentorship
  • Strong problem-solving focus

Key Requirements

  • Bachelor's degree in life sciences or business administration
  • Significant experience in clinical trial administration
  • Proven leadership skills managing teams
  • Experience within pharmaceutical or clinical research industry

Work Rights

Not specified

Tailored Resume

Cover Letter