Senior Medical Writer Regulatory Expertise

Overview

Elevate clinical documentation as a Senior Medical Writer at Precision Medicine Group. Lead development in compliance with industry standards, enhancing study quality and efficiency. You will capitalize on your 5+ years of medical writing experience, leading the creation of essential clinical documents across various studies.

• Write, edit, and ensure the timely delivery of high‑quality documents that meet regulatory requirements.
• Plan and produce clinical documents per regulatory guidelines.
• Ensure the document lifecycle is executed smoothly.
• Distill clinical data into transparent written content.
• Maintain and enhance medical writing processes.
• Engage in research to substantiate writing efforts.
• Solid writing and verbal communication skills enable you to work effectively with internal and external teams.

• BS degree in a relevant scientific field.
• 5+ years as a medical writer in CRO/sponsor settings.
• Proficiency in Microsoft and Adobe software.
• Thorough knowledge of ICH, FDA, and GCP.
• Impeccable attention to detail and ability to meet deadlines.

Unlock your potential in medical writing with Precision Medicine and drive impactful clinical studies.