Informed Consent Specialist Ii

ICON Clinical Research, LP

Mexico
Not specified; benefits include health insurance, ...
Informed consent form creation and optimization
Gcp and ethical guidelines knowledge
Stakeholder management with sponsors
This role involves leading the creation, review, and optimization of global and local informed consent forms in alignment with protocol and regulatory requirements

Job Summary

  • This role involves leading the creation, review, and optimization of global and local informed consent forms in alignment with protocol and regulatory requirements.
  • The successful candidate will interface with sponsors, ethics committees, and regulatory bodies to address queries and negotiate consent wording when required.
  • ICON offers a competitive salary along with benefits including health insurance, retirement planning, and a global Employee Assistance Programme.

Matching Summary

This role involves leading the creation, review, and optimization of global and local informed consent forms in alignment with protocol and regulatory requirements.

Salary

Not specified; Benefits include health insurance, retirement planning, and EAP

Skills & Requirements

Must-have

  • Informed consent form creation and optimization
  • GCP and ethical guidelines knowledge
  • Stakeholder management with sponsors
  • Translation process oversight
  • Patient-friendly writing skills

Nice-to-have

  • Mentorship of junior team members
  • Global regulatory expectations expertise
  • High-risk study experience
  • Template development capabilities

Key Requirements

  • Bachelor's degree in scientific or healthcare field
  • Significant clinical research experience
  • Strong focus on informed consent
  • Excellent writing and editing skills

Work Rights

Not specified

Tailored Resume

Cover Letter