Teams at Tarsus Pharmaceuticals

Leads outsourced nonclinical pharmacology studies across discovery and early clinical development. Responsibilities include study planning, CRO oversight, protocol and data review, study-result interpretation, regulatory documentation, and cross-functional collaboration. The role supports in vitro and in vivo efficacy, mechanism-of-action, proof-of-concept, GLP, and non-GLP programs while maintaining scientific rigor, data integrity, and regulatory readiness.

Leads cross-functional program management for a late-stage drug development program from Phase 2b/3 through regulatory submission, approval, and launch readiness. Responsibilities include integrated planning, pivotal trial coordination, regulatory filing execution, risk and scenario planning, governance, budget and resource tracking, stakeholder alignment, and continuous improvement. The role requires extensive biotech or pharmaceutical product development experience and strong program leadership skills.

Leads sales and launch growth for XDEMVY across an assigned eye-care territory. Builds relationships with ophthalmology and optometry customers, delivers disease-state education, manages accounts, navigates managed-care hurdles, analyzes performance data, executes business plans, and ensures compliant promotion. Collaborates with sales, marketing, medical affairs, market access, and other stakeholders while providing market feedback and driving territory results.