Informed Consent Writer

ICON

Not specified; not specified; competitive salary w...
Fully remote
Scientific knowledge of protocol structure
Health literacy writing skills
Ms office and adobe acrobat expertise
The Informed Consent Writer is responsible for preparing informed consent documents that disclose information about a clinical trial using health literate language

Job Summary

  • The Informed Consent Writer is responsible for preparing informed consent documents that disclose information about a clinical trial using health literate language.
  • ICON offers a competitive salary along with various benefits including health insurance, retirement planning, and a global employee assistance program.
  • The role requires working across multiple therapeutic areas while adhering to strict deadlines and collaborating with protocol authors and clinical teams.

Matching Summary

The Informed Consent Writer is responsible for preparing informed consent documents that disclose information about a clinical trial using health literate language.

Salary

Not specified; Not specified; Competitive salary with range of additional benefits

Skills & Requirements

Must-have

  • Scientific knowledge of protocol structure
  • Health literacy writing skills
  • MS Office and Adobe Acrobat expertise
  • Understanding of ICH regulatory guidance
  • American English fluency

Nice-to-have

  • Experience with structured content management
  • Collaborative authoring tool experience
  • Project management capabilities
  • Mentoring junior team members
  • Adaptability to new technologies

Key Requirements

  • Life sciences degree required
  • 3-5 years relevant experience preferred
  • Demonstrated experience translating scientific material

Work Rights

Not specified

Tailored Resume

Cover Letter