Join MMS as a Senior Nonclinical Writer, focusing on high-level technical documentation in a fully remote role. Drive the development of regulatory submissions and enhance your career.This full time position allows you to leverage 5+ years of pharmaceutical nonclinical writing experience. You will independently manage tasks involving writing eCTD submissions, Investigator’s Brochures, and Nonclinical Study Reports while collaborating with various departments to ensure scientific integrity.Key Responsibilities:
Author Module 2.4 and 2.6 eCTD submission documents
Interpret pharmacokinetics and toxicology data for submissions
Lead complex writing projects with minimal supervision
Work within various client systems and templates
Conduct meetings with clients and lead team discussionsRequirements:
Educational background in pharmacology or related field
Solid writing and analytical capabilities
At least 5 years of regulatory writing expertise
Proficient in MS Office and regulatory guidelines
Understanding of drug development processesMake a significant impact on clinical research by joining MMS today!#J-18808-Ljbffr

📌 Senior Nonclinical Writer For Pharmaceuticals Toronto
🏢 MMS Holdings
📍 Toronto