Start Up Specialist - 6 Month Assignment

ICON Clinical Research, LP

United Kingdom
Hybrid
Study start-up activities
Regulatory document preparation
Stakeholder coordination
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

  • 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, including clinical trial applications, ethics committee submissions, and regulatory agency communications.
  • ICON offers a range of additional benefits designed to be competitive within each country and focused on well-being and work-life balance opportunities.

Matching Summary

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

  • Study start-up activities
  • Regulatory document preparation
  • Stakeholder coordination
  • ICH-GCP knowledge
  • Project management skills

Nice-to-have

  • Process improvement initiatives
  • Fostering innovation and excellence
  • Inclusive environment

Key Requirements

  • Minimum 2 years experience
  • Bachelor's degree in life sciences
  • Study start-up experience
  • Local regulatory requirements knowledge
  • Willingness to travel 5%

Work Rights

Not specified

Tailored Resume

Cover Letter