Consultant I, Medical Writing - Remote

Overview

The MWS Consultant plays a critical role in authoring and managing regulatory documents, supporting client regulatory strategies, and ensuring high-quality deliverables that align with client expectations and regulatory standards.

In Short

• Author regulatory documents including Clinical Study Reports (CSRs) and study protocols.
• Lead development of complex regulatory modules.
• Ensure document accuracy and submission readiness.
• Track project timelines and adjust schedules.
• Facilitate client interactions and maintain trust.
• Collaborate with cross-functional teams.
• Provide guidance on document management systems.
• Engage in continuous learning and mentorship.

Requirements

• Advanced degree in a life or health science discipline preferred.
• Strong foundation in medical writing and regulatory writing.
• Exceptional project and time management skills.
• Strong critical thinking and data analysis skills.
• High attention to detail.
• Positive attitude toward feedback.
• Proficiency in Microsoft Office Suite.
• Knowledge of pharmaceutical environments.

Benefits

• Market competitive base salary and annual incentive plan.
• Robust benefit offerings.
• Flexible paid time off program.
• Flexible working hours.
• Fully remote or hybrid work options.