Commercial-stage oncology company focused on XPO1 inhibitor therapies
Karyopharm is a public pharmaceutical company developing XPO1-targeted cancer drugs across multiple indications. The tech stack leans heavily on Veeva (vault and broader suite) alongside standard enterprise tools—typical for regulated biotech—but the hiring profile is heavily weighted toward interns (11 of 20 open roles) paired with director-level positions, suggesting simultaneous scaling of entry-level execution and leadership structure. Active projects center on first-in-class combination launch, clinical supply chain, and regulatory readiness, while pain points cluster around disease awareness, operational efficiency, and cross-functional coordination.
Notable leadership hires: Business Director
Karyopharm Therapeutics is a public commercial-stage pharmaceutical company headquartered in Newton, MA, with 201–500 employees. The company develops novel cancer therapies targeting XPO1 inhibition across multiple indications: multiple myeloma, endometrial cancer, myelofibrosis, and diffuse large B-cell lymphoma (DLBCL). Operations span clinical research, drug development, regulatory affairs, and commercial functions. Current work includes manuscript preparation, clinical trial conduct, treatment landscape research, regulatory submissions, and quality assurance of approved products. The organization is actively hiring across healthcare, operations, research, and quality functions in the US and UK.
Karyopharm develops XPO1 inhibitor therapies for multiple myeloma, endometrial cancer, myelofibrosis, and diffuse large B-cell lymphoma (DLBCL). Current priorities include a first-in-class combination launch and quality assurance of Xpovio products.
Karyopharm uses Veeva Vault and the broader Veeva suite for regulatory compliance and document management, supplemented by JMP for statistical analysis, Zotero for reference management, and standard Microsoft Office and collaboration tools.
Karyopharm is headquartered in Newton, MA. The company is actively hiring in the United States and United Kingdom across clinical, research, operations, and quality functions.
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