Elevate your writing career with MMS as a Remote Senior Nonclinical Writer. This role focuses on developing complex nonclinical documents while collaborating with cross-functional teams. As a full time, remote Senior Nonclinical Writer at MMS, you will play a vital role in creating technical documents like eCTD submissions and Investigator’s Brochures.

You will work independently, ensuring alignment with regulatory guidelines while leveraging expertise in pharmacokinetics and toxicology data. Key Responsibilities:
Develop and write nonclinical submission documents for regulatory filings
Lead projects and manage writing independently with minimal oversight
Author documents based on technical sources and study data
Collaborate with project management and clinical teams
Guide others to complete complex writing projects Requirements:
BS in pharmacology, toxicology, biology, or chemistry
5+ years of nonclinical writing experience in pharmaceuticals
Expertise in GLP and regulatory guidelines
Proficiency in MS Office applications
Familiarity with clinical trial processes Bring your regulatory writing skills and become part of the cutting-edge team at MMS.

📌 Remote Senior Nonclinical Writer At Mms Toronto (Canada)
🏢 MMS Holdings
📍 Canada