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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…
Field-based role in Germany raising diagnosis rates of ADH1, a rare genetic cause of hypoparathyroidism, by building a network across hospital endocrinology departments, MVZs and office-based endocrinologists, sharing diagnostic pathways and supporting genetic testing ahead of a 2027 launch; planned to evolve into a Key Account Manager role after launch.
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 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.
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.
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.
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