Start Up Specialist - 6 Month Assignment

ICON plc

United Kingdom
Hybrid
Site start-up and activation experience
Regulatory document preparation and submission
Liaising with internal and external stakeholders
As a Study Start Up Specialist, you will lead the initiation of clinical trials, ensuring compliance with regulatory requirements, and contribute to the advancement of innovative treatments and therapies

Job Summary

  • As a Study Start Up Specialist, you will lead the initiation of clinical trials, ensuring compliance with regulatory requirements, and contribute to the advancement of innovative treatments and therapies.
  • Key responsibilities include leading the preparation and submission of regulatory documents, coordinating with stakeholders, and managing records.
  • ICON offers a competitive salary, various annual leave entitlements, health insurance, retirement planning, and a global employee assistance program.

Matching Summary

As a Study Start Up Specialist, you will lead the initiation of clinical trials, ensuring compliance with regulatory requirements, and contribute to the advancement of innovative treatments and therapies.

Skills & Requirements

Must-have

  • site start-up and activation experience
  • regulatory document preparation and submission
  • liaising with internal and external stakeholders
  • maintaining regulatory records
  • ICH-GCP and local regulatory requirements

Nice-to-have

  • process improvement initiatives
  • fostering an inclusive environment
  • driving innovation and excellence
  • well-being and work life balance

Key Requirements

  • Bachelor's degree in life sciences
  • Minimum 2 years clinical research experience
  • Specific study start-up activities experience
  • Willingness to travel 5%

Work Rights

Not specified

Tailored Resume

Cover Letter