Full-time
Associate Director, Regulatory Medical Writing
Posted by Regeneron Pharmaceuticals • United States, United States, United States
About the Role
As an Associate Director, Medical Writing, you will represent Medical Writing and provide leadership in one or more compound areas, oversees junior writers, and may assist in leading regulatory submissions. We work closely with senior Medical Writing management to help produce and ensure adherence to department guidelines, templates, standard timelines, and SOPs that follow regulatory guidelines. Responsibility will also include managing and developing staff; this may include performance management and training. Additionally, you will independently write all in-scope clinical documentation in their compound areas.
**This position can be either fully remote or can be on-site at our Sleepy Hollow, NY or Warren, NJ offices.**
**A typical day may include the following:**
• Leads all MW deliverable work for assigned compounds/indications
• Manages work of both internal and outsourced Medical Writers
• Works with clinical team to develop document strategy and write...
**This position can be either fully remote or can be on-site at our Sleepy Hollow, NY or Warren, NJ offices.**
**A typical day may include the following:**
• Leads all MW deliverable work for assigned compounds/indications
• Manages work of both internal and outsourced Medical Writers
• Works with clinical team to develop document strategy and write...
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