Find clinical, allied health, care team, and healthcare operations openings using one smart search field across cities, regions, and employers.
Johnson & Johnson Innovative Medicine
Overview
Develops and coordinates clinical and regulatory documents, including protocols and clinical study reports, within the oncology therapeutic area. Collaborates with cross-functional teams to establish document timelines and ensure adherence to internal standards and regulatory guidelines.
Quick view →
Compensation
CA$74,000 - CA$119,600 / YEAR
Posted
4 days ago
ICON plc
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.
Salary not listed
21 days ago
