Blog writer • odessa tx
As a medical writer on this project, you would own a part in multiple workflows: 1.Clinical Data Generation — we need to generate and validate high-quality, synthetic clinical trial data.CSR task a... Show more
As a medical writer on this project, you would own a part in multiple workflows: 1. Clinical Data Generation — we need to generate and validate high-quality, synthetic clinical trial data. 2. CSR task authorship — you must be capable of authoring full CSR sections, and designing prompts, golden outputs, and rubrics to quantify the ability of an AI agent attempting to do the same thing. To be qualified for this role, you must fit the following requirements: - Location: US, Canada, or France. - YOE: 5+ required. 10-25 preferred. - Education: PhD, or equivalent. - Hourly availability: 20-25 hours/week, minimum. 30+ preferred. - Experience: **MUST** have experience working with pre-market (Phases 1-3) clinical trial data and report authorship. Comfortable with full-document, long-horizon authorship.