Associate Director, Clinical Regulatory Writing - Onsite Boston
$75 - $85 per hourThe Fountain Group
The Fountain Group is seeking a Clinical Regulatory Writing Associate Director in Boston, MA. This role focuses on managing regulatory writing activities for complex drug development projects, requiring strong leadership skills and extensive experience in medical writing. The ideal candidate will have a Master’s degree (PhD preferred) along with 4–5+ years in regulatory writing within the pharma or biotech industries. This position is 100% onsite with a competitive salary ranging from $75 to $85 per hour. #J-18808-Ljbffr The Fountain Group
Vacancy posted 12 hours ago
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