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 discussions
Requirements: • Educational background in pharmacology or related field • Strong writing and analytical capabilities • At least 5 years of regulatory writing expertise • Proficient in MS Office and regulatory guidelines • Understanding of drug development processes
Make a significant impact on clinical research by joining MMS today!