Informed Consent Writer

Job Summary

A company is looking for an Informed Consent Writer responsible for preparing informed consent documents for clinical trials.

Key Responsibilities

• Read and understand clinical trial protocols to prepare informed consent documents
• Collaborate with protocol authors to ensure accurate documentation and adherence to timelines
• Manage informed consent writing projects and participate in clinical trial team meetings

Required Qualifications

• Life sciences degree
• 3-5 years of relevant experience in medical writing or related fields
• Understanding of clinical trial operations and informed consent requirements
• Technical expertise in MS Office and document management systems
• Ability to work independently and collaboratively in a deadline-driven environment