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 projectsRequirements:
- 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 processesBring your regulatory writing skills and become part of the innovative team at MMS.#J-18808-Ljbffr

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