Associate Director, Clinical Medical Writing

Company Name

BioMarin Pharmaceutical Inc.

Job Overview

The Associate Director of Clinical Medical Writing oversees Medical Writing staff, authoring and editing regulatory submission documents and publications. Responsibilities include departmental resource planning, submission planning, and budget management. The role involves acting as a management-level author/reviewer, building cross-functional partnerships, and managing outsourced projects.

Key Responsibilities

• Drafting and editing clinical study protocols
• Creating clinical study reports (CSRs)
• Developing investigator's brochures
• Preparing regulatory filing documents

Requirements

• Master's degree (preferred)
• At least 10 years of medical writing experience in pharma
• A minimum of 3 years of management experience