Senior Scientific Writer - job 1 of 2

Job Summary

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