Not specified; not specified; competitive benefits...
Fully remote
Health literacy document preparation
Clinical trial protocol understanding
Ich regulatory guidance knowledge
The Informed Consent Writer is responsible for preparing informed consent documents that disclose information about a clinical trial using health literate language to help candidates make an informed decision
Job Summary
The Informed Consent Writer is responsible for preparing informed consent documents that disclose information about a clinical trial using health literate language to help candidates make an informed decision.
ICON offers a competitive salary along with a range of benefits including various annual leave entitlements, health insurance offerings, and retirement planning options.
The role requires the ability to work in a deadline-driven environment while collaborating independently and with teams across multiple therapeutic areas.
Matching Summary
The Informed Consent Writer is responsible for preparing informed consent documents that disclose information about a clinical trial using health literate language to help candidates make an informed decision.
Salary
Not specified; Not specified; Competitive benefits package including health insurance and retirement planning
Skills & Requirements
Must-have
Health literacy document preparation
Clinical trial protocol understanding
ICH regulatory guidance knowledge
MS Office and Adobe Acrobat expertise
American English fluency
Nice-to-have
Structured content management concepts
Collaborative authoring tool experience
Project management skills
Coaching junior team members
Tool development participation
Key Requirements
Life sciences degree required
3-5 years relevant experience preferred
Demonstrated experience translating scientific material