Medical Writer - Remote

Overview

We are seeking an experienced, collaborative, detail-oriented medical writer with a passion for medical writing. The successful candidate will lead the planning, authoring, reviewing, and QC of clinical and regulatory documents.

In Short

• Lead the planning and authoring of clinical and regulatory documents.
• Review and ensure quality control of documents.
• Collaborate with cross-functional subject matter experts.
• Work independently to develop high-quality, scientifically accurate documents.
• Oversee the work of contract writers.
• Contribute to medical writing process development.
• Passion for medical writing.
• Detail-oriented and collaborative approach.
• Experience in the biotechnology or pharmaceutical industry.
• Strong communication skills.

Requirements

• Proven experience in medical writing.
• Strong understanding of clinical and regulatory documentation.
• Ability to work with cross-functional teams.
• Excellent writing and editing skills.
• Detail-oriented with a focus on quality.
• Experience overseeing contract writers is a plus.
• Knowledge of the biotechnology industry.
• Ability to manage multiple projects simultaneously.
• Strong organizational skills.
• Ability to work independently and as part of a team.

Benefits

• Opportunity to work in a leading biotechnology company.
• Collaborative work environment.
• Contribute to meaningful medical advancements.
• Professional development opportunities.
• Competitive salary and benefits package.
• Work with a passionate team.
• Flexible work arrangements.
• Access to cutting-edge research.
• Supportive company culture.
• Engagement in innovative projects.