Job Summary

A commercial-stage cancer biotechnology company has an open position for a Remote Senior Medical Writer.

Must be able to:

• Write, edit, and format clinical regulatory documents that conform to domestic and/or international regulatory submission
• Manage timelines and communicate to maintain awareness of expectations, milestones, and deliverables
• Review and edit documents, including those authored by others both internally and externally

Qualifications Include:

• At a minimum, a BA/BS degree; PhD/PharmD in life sciences preferred
• At least 3-5 years of relevant industry experience as a regulatory medical writer
• Demonstrated ability to communicate and write English clearly, concisely
• Well-organized: ability to prioritize tasks, work simultaneously on multiple projects
• Excellent interpersonal skills; a team player
• All other requirements necessary for this position