Senior Medical Writer - Remote

Overview

The Senior Medical Writer will be responsible for writing and editing clinical development documents while working remotely from any location in South Africa.

In Short

• Home-based role in South Africa.
• Requires medical writing experience.
• Write and edit various clinical documents.
• Maintain timelines and workflow of writing assignments.
• Interact directly with clients to coordinate projects.
• Mentor other medical writers.
• Must have at least 3-5 years of regulatory writing experience.
• Substantial Oncology experience required.
• Exceptional writing and organizational skills are essential.
• Expert in MS Word, Excel, and PowerPoint.

Requirements

• 3 years of experience in the pharmaceutical industry.
• Bachelors, Masters, or Ph.D. in a scientific or medical discipline.
• Experience leading and managing teams.
• Strong understanding of federal regulations and clinical data.
• Experience with regulatory submissions is a plus.

Benefits

• Work from home flexibility.
• Opportunity to work with a leading CRO.
• Mentorship opportunities.
• Engagement in meaningful projects in the pharmaceutical industry.