Informed Consent Specialist Ii

ICON Clinical Research, LP

Mexico City, Mexico
Informed consent document development
Global clinical trial oversight
Gcp and ethical guidelines knowledge
ICON plc is a world-leading healthcare intelligence and clinical research organization focused on shaping the future of clinical development

Job Summary

  • ICON plc is a world-leading healthcare intelligence and clinical research organization focused on shaping the future of clinical development.
  • Your role will involve 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.

Matching Summary

ICON plc is a world-leading healthcare intelligence and clinical research organization focused on shaping the future of clinical development.

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 inclusive environment
  • Work-life balance focus

Key Requirements

  • Bachelor's degree in relevant discipline
  • 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

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