Advanced medical degree (MD, DO, PharmD, or PhD). 3+ years of medical affairs experience in the Pharmaceutical/Biotechnology industry. Experience in hypertension, sleep apnea, or chronic kidney disease is preferred. Launch experience is preferred. Experience in budget and vendor management. Proven success in a fast-paced, entrepreneurial, smaller company environment is highly desired. Proven experience in working collaboratively and cross-functionally. Demonstrated understanding of laws, regulations, standards, and guidance governing publications. Proven experience collaborating with cross-functional, international teams. Strong understanding of compliance and regulatory frameworks governing scientific exchange. Strong understanding of regulatory requirements (e.g., FDA, EMA) and industry standards (e.g., GPP, ICH, PhRMA Code).