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Mavericks Wanted When was the last time you achieved the impossible? If that thought feels overwhelming, you might want to pause here, but if it sparks excitement...read on In 2015, we pioneered a “moneyball for…
Oversee pharmacovigilance quality and compliance for a biopharma company, ensuring adherence to global regulations and managing regulatory inspections.
Leads go-to-market strategy and portfolio planning for a rare-disease drug portfolio, translating market insight into commercial roadmaps and investment priorities.
Lead pharmacometric strategies and modeling for pediatric drug development, authoring regulatory documents and guiding global trials to optimize dosing and safety.
Leads cross-functional CMC/QA teams to coordinate biopharma manufacturing, regulatory filings, and vendor contracts while managing CDMOs and timelines for rare-disease drug development.
Lead clinical development for rare-disease therapies, designing and overseeing trials, ensuring patient safety, and guiding regulatory strategy for chronic hypoparathyroidism programs.
Lead strategic planning and commercial launch readiness for a rare-disease drug program, using financial modeling and cross-functional collaboration to guide biopharma decisions.
Lead international health economics and outcomes research to secure reimbursement for rare-disease therapies, designing value dossiers and real-world evidence studies while engaging HTA bodies like NICE and G-BA.
Design and execute integrative computational analyses of multiomics datasets to accelerate therapeutic discovery in rare genetic diseases, leveraging AI-enabled approaches and collaborating with cross-functional scientists.
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Sequoia