Start Up Specialist - 6 Month Assignment

ICON Broadbean

United Kingdom
Hybrid
Site start-up and activation experience
Regulatory document preparation
Stakeholder coordination and liaison
As a Study Start Up Associate II at ICON, 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 Associate II at ICON, you will lead the initiation of clinical trials, ensuring compliance with regulatory requirements, and contribute to the advancement of innovative treatments and therapies.
  • You will contribute to site start-up and activation activities, taking responsibility for your deliverables and working collaboratively.
  • 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 Study Start Up Associate II at ICON, 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
  • stakeholder coordination and liaison
  • record management for submissions
  • ICH-GCP and local regulatory knowledge

Nice-to-have

  • process improvement initiatives
  • foster an inclusive environment
  • drive innovation and excellence
  • support study teams on best practices

Key Requirements

  • Bachelor's degree in life sciences
  • Minimum of 2 years clinical research experience
  • Specific experience in study start-up
  • Excellent organizational and project management skills
  • Excellent communication and interpersonal skills
  • Willingness to travel as required (approximately 5%)

Work Rights

Must be based in the UK

Tailored Resume

Cover Letter