Axsome Therapeutics is a biopharmaceutical company committed to developing therapies to improve the lives of patients. We are cultivating a creative and entrepreneurial work environment as we continue to grow as an organization. We invite you to review our current employment opportunities listed below.
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.
Current Employment Opportunities
Clinical Research Associate: In-HouseNew York, NY
The CRA is responsible for supporting the organization to successfully develop and implement clinical trials across its product candidate portfolio and development pipeline. For each assigned study, the CRA is responsible for: conducting site evaluation visits, managing the site startup process, leading site initiation activities, building site relationships, conducting remote data review and on-site monitoring, ensuring proper site closeout and database lock. This position plays a key role to ensure the successful execution of clinical studies in accordance with SOPs, FDA and other regulatory authority regulations, GCP, and ICH guidelines.
Clinical Trials AssistantNew York, NY
The Clinical Trials Assistant is responsible for supporting the organization to successfully develop and implement clinical trials across its product portfolio and development pipeline. The Clinical Trial Assistant provides a key support function to the clinical operations team. Under general guidance from Clinical Operations, you will support the Clinical team responsible for management of multiple clinical trials (all phases), and assure compliance with SOPs, FDA regulations, GCP and ICH guidelines.
Sr. / Clinical Research Associate (West Coast)Remote
The CRA will be responsible for site management and monitoring activities at assigned sites across assigned programs ensuring the trial is conducted in compliance with the protocol, ICH/GCP, applicable regulatory requirements and applicable SOPs/Work Instructions. Additional responsibilities will include in-house data review and occasionally leading the planning and development of study set-up.