Associate Medical Writer
Core
Assist with preparing high-quality medical and scientific documents including Informed consent forms, Lay summaries, and clinical/program level documents for internal and external clients.
Role type
Associate Medical Writer
Builds
Regulatory and patient-centric clinical documentation
Domain
Pharmaceutical/Biotech
Deliverable
production ML models | product features | dashboards & analysis | research | client delivery | infrastructure | physical/clinical work
Required skills
Medical writing, editing, proofreading, regulatory documentation knowledge, drug development process knowledge, data interpretation, project management basics
Preferred skills
Pharmaceutical/CRO industry experience, scientific writing experience
Technologies
Document management systems, Excel, Outlook
Responsibilities
Research, write, and edit routine patient-centric documents; assist with complex clinical and scientific documents; ensure compliance with quality processes; assist in program management activities like developing timelines and budgets; participate in project launch and review meetings.
