Senior Regulatory Submissions Medical Writer

The role

You'll sit alongside a Clinical Scientist on a sponsor-dedicated team, writing clinical study protocols and protocol amendments for late-development oncology, hematology and cell therapy work. The role is remote from the US or Canada, with travel of less than 25% possible. You need 3-5 years of medical writing with proven protocol experience, and Veeva or CARA experience is listed.

Tools and skills