Find clinical, allied health, care team, and healthcare operations openings using one smart search field across cities, regions, and employers.
ICON plc
Overview
The Informed Consent Writer is responsible for creating health-literate informed consent documents for clinical trials across various therapeutic areas. This includes collaborating with protocol authors and managing the design and planning of documentation to ensure timely delivery and regulatory compliance.
Quick view →
Compensation
Salary not listed
Posted
22 days ago
Alimentiv
Manage Trial Master File (TMF) content and processes throughout the study lifecycle from setup to archiving. Ensure the TMF is inspection-ready by performing periodic reviews, reconciling document lists, and collaborating with cross-functional study teams.
23 days ago
