Associate Director of Medical Writing - job 2 of 2

Job Summary

A company is looking for an Associate Director, Medical Writing.

Key Responsibilities

• Author and deliver high-quality clinical and regulatory documents in collaboration with cross-functional team members
• Coordinate document development, review, and approval while managing timelines and vendor relationships
• Contribute to process improvements and ensure document compliance with company and regulatory guidelines

Required Qualifications and Education

• Bachelor's degree in a relevant discipline; PhD in molecular biology, genetics, or related field preferred
• 5+ years of experience in the pharmaceutical/biotechnology industry as a medical writer
• Experience in oncology is preferred but not required
• Knowledge of drug development, clinical research, and regulatory requirements
• Strong project management and organizational skills