We are seeking a Medical Writer to lead the creation of regulatory submission documents.
About this role
* Manage medical writing activities, including clinical study protocols and ensure adherence to regulatory standards.
This is an opportunity for experienced medical writers with strong knowledge of FDA regulations. The ideal candidate has 3-5 years of experience in medical writing and should be comfortable working independently as well as part of a team.
Key qualifications
* Bachelor's degree or higher in a relevant field (e.g., life sciences, English).
- Visionary Regulator Submission Specialist – Clinical Study Protocol ],