Medical Writing Operations Manager

Job Summary

A company is looking for a Medical Writing Operations Manager III.

Key Responsibilities

• Manage and support projects in accordance with established processes and SOPs, ensuring timelines are met
• Provide project management and editorial assistance for scientific and regulatory documents related to drug development
• Lead or support Medical Writing process improvement initiatives and manage the development of SOPs and templates

Required Qualifications

• Bachelor's degree in life sciences, professional/technical writing, or related field
• Minimum of 5 years of experience in pharmaceutical/biotech regulatory document preparation/management
• Solid understanding of the clinical development process and pharmaceutical project management principles
• Experience with technical writing and quality control for regulatory submissions
• Familiarity with electronic document management systems and advanced proficiency in Microsoft Office software