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

Bachelor’s degree required
5 years or more of Regulatory Operations experience
Understanding of eCTD requirements, FDA electronic gateway submissions, and FDA guidance documents
Operational experience supporting investigational and/or marketed products (INDs/CTAs, NDAs/MAAs)
Ability to work on site Monday, Tuesday & Thursday. We are unable to consider candidates who are looking for fully remote roles

Experience, Knowledge and Skills

Prior experience with regulatory document publishing and submission
Prior experience with regulatory information management systems
Proficiency with Microsoft Office Suite and Adobe Acrobat
Strong attention to detail and excellent organization skills
Exceptional time-management skills
Strong interpersonal skills
Comfortable multi-tasking in a fast-paced small company environment and able to adjust workload based upon changing priorities

Salary and Benefits:

The anticipated salary range for this role is $120,000 - $150,000. We encourage candidates of all levels to apply as there may be flexibility on final job title and responsibilities. The salary offer will be based on a variety of factors, including experience, qualifications, internal equity and location. Axsome offers a competitive employment package that includes an annual bonus, significant equity and a generous benefits package.

Axsome is committed to equal employment opportunity and providing reasonable accommodations to applicants with physical and/or mental disabilities. We value and encourage diversity and solicit applications from all qualified applicants without regard to race, color, gender, sex, age, religion, creed, national origin, sexual orientation, gender identity, ancestry, citizenship, marital status, physical or mental disability, medical condition, veteran status, genetic information, or any other characteristic protected by federal, state, or local law.

Axsome Therapeutics does not accept unsolicited resumes from recruiters or third-party recruitment agencies and will not pay placement fees for unsolicited candidates that are sent to hiring managers, the HR team or other Axsome team members. Only approved vendors who have been explicitly asked to support a specific search will receive access to our Applicant Tracking System to submit candidates for consideration.

Manager/Senior Manager, Regulatory Affairs Operations