Manager/Senior Manager, Regulatory Affairs Operations

Axsome Therapeutics is a biopharmaceutical company leading a new era in the treatment of central nervous system (CNS) conditions. We deliver scientific breakthroughs by identifying critical gaps in care and develop differentiated products with a focus on novel mechanisms of action that enable meaningful advancements in patient outcomes. Our industry-leading neuroscience portfolio includes FDA-approved treatments for major depressive disorder, excessive daytime sleepiness associated with narcolepsy and obstructive sleep apnea, and migraine, and multiple late-stage development programs addressing a broad range of serious neurological and psychiatric conditions that impact over 150 million people in the United States. Together, we are on a mission to solve some of the brain’s biggest problems so patients and their loved ones can flourish. For more information, please visit us at www.axsome.com and follow us on LinkedIn and X.

About This Role:

Axsome Therapeutics is seeking a Manager/Senior Manager, Regulatory Operations.  Level will be commensurate with prior Regulatory Operations experience. The role is responsible for managing regulatory operations necessary to ensure the successful preparation and filing of regulatory submissions for multiple product candidates. The right candidate will have knowledge of the regulatory requirements for electronic submissions and prior experience with publishing of regulatory submission, electronic document management, and regulatory information management (RIM) systems. This role reports to the Executive Director, Regulatory Affairs.

This role is based at Axsome’s HQ in New York City with an on-site requirement of at least three days per week. We are unable to consider candidates who are looking for fully remote roles.

JOB RESPONSIBILITIES

• Publish electronic submissions: compile and generate submission packages, validate submission, and address any warnings or errors before submission
• Coordinate internal publishing activities
• Finalize regulatory documents for electronic submission by verifying document completeness and applying formatting standards
• Provide training and support for publishing and electronic document management systems
• Track submission statuses and maintain logs of submission sequences, dates, and acknowledgments
• Archive health authority communications and submissions, including storing published packages and validation reports
• Work closely with document authors, reviewers, and regulatory leads to ensure timely and high quality submission
• Manage vendors in support of electronic publishing and other aspects of regulatory operations
• Additional responsibilities as assigned

QUALIFICATIONS