MindMed is a company that specializes in developing innovative treatments for brain health disorders. It utilizes rigorous scientific methods to create a pipeline of product candidates, particularly focusing on the therapeutic potential of psychedelics and other novel compounds. These treatments aim to address unmet patient needs in areas such as Generalized Anxiety Disorder (GAD), Major Depressive Disorder (MDD), and Autism Spectrum Disorder (ASD). MindMed is committed to advancing the research and development of these therapies, although they are not yet approved by the FDA or other health authorities, meaning their safety and efficacy are still under evaluation.
51 - 200 employees
Founded 2019
๐งฌ Biotechnology
๐ Pharmaceuticals
๐ฌ Science
๐ฐ $30M Post-IPO Equity on 2022-09
6 days ago
๐บ๐ธ United States โ Remote
๐ต $140k - $173.1k / year
โฐ Full Time
๐ Senior
๐ง QA Engineer (Quality Assurance)
MindMed is a company that specializes in developing innovative treatments for brain health disorders. It utilizes rigorous scientific methods to create a pipeline of product candidates, particularly focusing on the therapeutic potential of psychedelics and other novel compounds. These treatments aim to address unmet patient needs in areas such as Generalized Anxiety Disorder (GAD), Major Depressive Disorder (MDD), and Autism Spectrum Disorder (ASD). MindMed is committed to advancing the research and development of these therapies, although they are not yet approved by the FDA or other health authorities, meaning their safety and efficacy are still under evaluation.
51 - 200 employees
Founded 2019
๐งฌ Biotechnology
๐ Pharmaceuticals
๐ฌ Science
๐ฐ $30M Post-IPO Equity on 2022-09
โข MindMed is a clinical stage biopharmaceutical company developing novel product candidates to treat brain health disorders. โข Responsibilities include supporting GCP QA needs, conducting audits, and ensuring compliance with regulations. โข Requires independent working in a geographically distributed team and managing multiple priorities.
โข 7+ years working in GCP Quality Assurance and Clinical Program Management โข BA in scientific field, or BA in non-science field with additional 2 years relevant work experience โข Documented training on and knowledge of current FDA Regulations and GCPs โข Experience in conducting, reporting, responding to GCP vendor audits, clinical investigator audits, and protocol and report audits โข Proficient written and verbal communication skills โข Ability to collaborate effectively with cross functional team members and external partners โข A can-do attitude and excellent attention to detail โข This person may travel, domestically and internationally, up to 25% of the time
โข 100% paid health benefits including Medical, Dental and Vision for you and your dependents โข 401(k) program with company match and immediate vesting โข Flexible time off โข Generous parental leave and some fun fringe perks!
Apply Now6 days ago
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