Informed Consent Writer

ICON plc

Competitive salary; benefits: various annual leave...
Fully remote
Understanding of protocol structure and design
Ability to translate scientific material for lay audience
Knowledge of ich and regulatory guidance
The Informed Consent Writer is responsible for preparing informed consent documents using health literate language to help candidates make informed decisions about trial participation

Job Summary

  • The Informed Consent Writer is responsible for preparing informed consent documents using health literate language to help candidates make informed decisions about trial participation.
  • ICON plc offers a competitive salary along with various benefits including health insurance, retirement planning, and global employee assistance programs.
  • Candidates must demonstrate the ability to prepare summaries of clinical trial designs for lay audiences while adhering to established guidelines and governmental regulations.

Matching Summary

The Informed Consent Writer is responsible for preparing informed consent documents using health literate language to help candidates make informed decisions about trial participation.

Salary

Competitive salary; Benefits: Various annual leave, health insurance, retirement planning, EAP; Not specified

Skills & Requirements

Must-have

  • Understanding of protocol structure and design
  • Ability to translate scientific material for lay audience
  • Knowledge of ICH and regulatory guidance
  • Technical expertise in MS Office and Adobe Acrobat
  • Experience with document management systems

Nice-to-have

  • Strong project management skills
  • Collaborative team work environment
  • Adaptability to new tools and technology
  • Customer focus orientation
  • Mentoring junior team members

Key Requirements

  • Life sciences degree required
  • 3-5 years of relevant experience preferred
  • Complete fluency in American English reading and writing

Work Rights

Not specified

Tailored Resume

Cover Letter