Principal Medical Writer leading CMC regulatory submissions for Veristat’s life - sciences clients. Authoring Modules 3 and 2.3 while guiding project teams and mentoring regulatory writers.
About the role
- Medical Writer generating synthetic clinical trial data and authoring CSRs. Helping Mercor train frontier AI models through expert clinical documentation.
Responsibilities
- Own workflows for generating and validating high-quality synthetic clinical trial data
- Author full clinical study report (CSR) sections
- Design prompts, golden outputs, and rubrics to quantify AI-agent performance
- Work on projects training and enhancing AI systems
- Collaborate with leading researchers and AI labs
Requirements
- Location: US, Canada, or France
- 5+ years of experience required; 10–25 years preferred
- PhD or equivalent
- Availability of at least 20–25 hours per week; 30+ preferred
- Experience working with pre-market (Phases 1–3) clinical trial data
- Experience authoring clinical trial reports and full CSR sections
- Ability to design prompts, golden outputs, and rubrics for evaluating AI agents
- Comfortable with full-document, long-horizon authorship
- Must work as an independent contractor
- H1-B and STEM OPT candidates are not supported
Benefits
- Fully remote role with flexible scheduling
- Weekly payments via Stripe or Wise
- Competitive pay
- Opportunity to collaborate with leading researchers
- Opportunity to help shape next-generation AI systems
- Referral bonus of up to $600 per successful referral
- Reasonable accommodations upon request
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