Informed Consent Specialist Ii

ICON

Mexico City, Mexico
Informed consent document development
Global clinical trial oversight
Gcp and ethical guidelines knowledge
As an Informed Consent Specialist II at ICON, you will take a lead role in the development, review, and oversight of informed consent documents for complex, global clinical trials

Job Summary

  • As an Informed Consent Specialist II at ICON, you will take a lead role in the development, review, and oversight of informed consent documents for complex, global clinical trials.
  • Key responsibilities include leading the creation, review, and optimization of global and local informed consent forms (ICFs) in alignment with protocol, regulatory, and sponsor requirements.
  • 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 an Informed Consent Specialist II at ICON, you will take a lead role in the development, review, and oversight of informed consent documents for complex, global clinical trials.

Skills & Requirements

Must-have

  • Informed consent document development
  • Global clinical trial oversight
  • GCP and ethical guidelines knowledge
  • Patient-friendly language writing
  • Stakeholder management and communication

Nice-to-have

  • Mentorship of junior team members
  • Driving standardization and efficiency
  • Fostering an inclusive environment
  • Focus on well-being and work-life balance

Key Requirements

  • Bachelor's degree in relevant field
  • Significant clinical research experience
  • In-depth knowledge of GCP
  • Excellent writing and editing skills
  • Proven ability to manage multiple studies

Work Rights

Not specified

Tailored Resume

Cover Letter