Job Description:

• Transform complex clinical topics, product narratives, and company perspectives into clear, credible, high-quality content.
• Lead the drafting of blogs, thought leadership, case studies, and research-driven pieces.
• Convert core messages into fit-for-purpose copy across web, email, social, and promotional materials.
• Translate complex clinical, regulatory, or access-related topics into clear, responsible communication for diverse audiences.
• Maintain exceptional writing standards, claims sensitivity, and sound editorial judgment in a highly regulated environment.
• Partner with internal subject matter experts to turn rough or incomplete inputs into strong, review-ready drafts.
• Responsibly use AI tools to accelerate drafting, editing, and repurposing without compromising originality or factual accuracy.

Requirements:

• Proven experience and deep understanding of clinical trials, expanded access, drug development, or the BioPharma/health-tech landscape.
• 5+ years in content writing, copywriting, or editorial roles, with a strong portfolio of long-form and multi-channel work.
• Native-level written English with the ability to simplify technical jargon without losing its authority.
• A disciplined approach to claims, accuracy, and creating 'review-ready' content for a regulated space.
• Experience using AI tools for research and efficiency, alongside an understanding of SEO/AEO (Answer Engine Optimisation).

Benefits:

• Competitive salary, annual performance bonus, and an Employee Stock Option Plan.
• 401K: Every US employee will be automatically enrolled in a 401(K) retirement plan.
• Paid time off: 25 days per year for full-time employees.
• Sick leave: 5 days/ year at 100% paid.
• Great career development opportunities in a fast-growing company.
• Learning and development budget alongside internal knowledge sharing sessions.