Skip to main content
Viking Therapeutics, Inc. is seeking a Medical Writer to plan, author, edit, and finalize clinical and regulatory documents across our GLP-1/GIP programs. You will collaborate with Clinical Development, Biostatistics, Regulatory Affairs, and external CROs to produce study protocols, CSRs, IBs, and submission-related sections. The role requires 4+ years in regulatory/clinical medical writing, a life sciences degree, and strong writing skills.

Also on the board Same function, level within a rung

Level

Senior

Location

San Diego, CA

Occupation

Writers and Authors

Industry

Biological Product Manufacturing

Posted

today

Apply for this role (opens in a new tab)