Senior Scientific Writer

A company is looking for a Senior Scientific Writing Specialist to draft and manage regulatory submission documents for nonclinical pharmacology. Key Responsibilities Independently author nonclinical documents for submission to health authorities worldwide Drive document review cycles and participate in the revision and maintenance of document templates Adhere to timelines for document preparation and manage multiple projects simultaneously Required Qualifications Basic understanding of eCTD and the drug development process; GLP experience is a plus Proficiency in computer applications such as Word, Excel, and Adobe Fluency in English Passion for science and teamwork

Jun 10, 2025 - 12:10

A company is looking for a Senior Scientific Writing Specialist to draft and manage regulatory submission documents for nonclinical pharmacology. Key Responsibilities Independently author nonclinical documents for submission to health authorities worldwide Drive document review cycles and participate in the revision and maintenance of document templates Adhere to timelines for document preparation and manage multiple projects simultaneously Required Qualifications Basic understanding of eCTD and the drug development process; GLP experience is a plus Proficiency in computer applications such as Word, Excel, and Adobe Fluency in English Passion for science and teamwork