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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…
Lead biostatistics and AI integration for clinical trials, designing statistical methods and embedding AI/ML tools into regulated biopharma workflows while ensuring GxP compliance.
Lead strategic finance and capital markets efforts for a biotech company, evaluating M&A, licensing, and financings to accelerate rare-disease drug development.
Leads commercial analytics and portfolio intelligence for a biotech company, translating complex scientific and financial data into strategic recommendations for executives and the board.
Leads biostatistics for medical publications and external scientific communications, designing analyses, developing statistical plans, and collaborating with cross-functional teams to deliver publication-ready insights in rare disease drug development.
Leads omnichannel analytics strategy for BridgeBio’s marketing and promotional initiatives, analyzing HCP/patient data to optimize campaigns, define KPIs, and drive insights for channel investments across digital and field-based efforts in rare disease therapeutics.
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.
Oversee quality assurance for drug product manufacturing at contract manufacturers, reviewing batch records, ensuring cGMP compliance, and managing quality events for a biopharma company.
Lead strategic planning and commercial launch readiness for a rare-disease drug program, using financial modeling and cross-functional collaboration to guide biopharma decisions.
Leads cross-functional teams to create clear, executive-ready commercial reports for biotech leadership, translating complex data into strategic narratives for Board and C-suite decisions.
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Sequoia