Associate Director, Medical Writing

The Associate Director, Medical Writing will author, edit and provide input to documents required for regulatory submissions to US and other global health authorities, presentations, posters, publications and regulatory fulfillment.

Requirements

• Bachelor’s degree required, PhD in advanced medical or life sciences or a related area degree preferred (e.g., MS, Ph.D.) with 8+ years of experience in the life sciences industry or an equivalent combination of academic and industry experience
• Extensive recent hands-on oncology experience, preferably within targeted oncology programs
• Demonstrated, recent hands-on experience authoring regulatory designation submissions from inception, including Orphan Drug, Fast Track and Breakthrough Therapy applications

Benefits

• Group healthcare plans that offer medical, dental, vision, and basic life and AD&D insurance
• Short-term and long-term disability insurance
• Flexible spending accounts
• Health savings account
• Voluntary insurance programs including voluntary life and AD&D accident, and critical illness
• 401(k) plan
• 10 hours of paid vacation time every month
• Paid sick leave for every 30 hours worked
• 17 paid holidays, including a winter closure, throughout the calendar year