Own sales execution and account development across an eye-care territory, educating customers on disease states and XDEMVY while driving launch growth, compliant promotion, and strong customer relationships.
Tarsusrx jobs
Develops treatments for patients in need.
27 open roles at Tarsusrx
Plan and oversee nonclinical pharmacology studies across drug-development programs, leading outsourced execution, interpreting results, and contributing scientific analysis and documentation for regulatory decisions.
Leads oral drug-product formulation and process development from preclinical stages through Phase 3 and registration readiness, directing internal teams and external partners while advancing scalable manufacturing and regulatory plans.
Leads cross-functional planning and execution for a late-stage drug development program, coordinating pivotal trials, regulatory submissions, risk mitigation, and launch readiness through approval and commercialization.
Leads global clinical supply strategy and execution across development programs, overseeing forecasting, packaging, distribution, inventory, vendor performance, compliance, budgets, and team development to ensure investigational products.
The Medical Science Liaison leads compliant scientific exchange with eye-care professionals, educates practices on disease states, gathers field insights to inform medical strategy, and supports medical affairs initiatives.
Own sales execution and account development across an eye care territory, educating customers on disease states and driving the launch and growth of XDEMVY through compliant, data-informed selling.
Leads global regulatory strategy for assigned drug development projects, guiding US pre- and post-approval activities, regulatory submissions, cross-functional planning, and regulatory team development.
Leads pharmacology and translational strategy across discovery and early clinical development, shaping asset decisions, evaluating mechanisms and disease models, and building cross-functional and external partnerships.
Direct pharmacokinetics and DMPK strategy across drug discovery and clinical development, guiding studies, dose selection, regulatory submissions, and cross-functional decisions with PK/PD insights.
Manage eye-care KOL relationships and compliant scientific exchange, deliver disease-state education, gather field insights to shape medical strategy, and support medical affairs initiatives across an assigned territory.
Leads alliance management capabilities and strategic partnerships, ensuring development and commercial milestones are met while coordinating R&D due diligence and integration planning for potential assets and collaborations.
Lead territory sales for XDEMVY by educating eye care customers, building account relationships, executing launch and growth plans, and achieving sales goals while maintaining compliance.
Own territory sales execution and account development for XDEMVY, educating eye care customers, building stakeholder relationships, navigating managed care, and driving compliant product launch growth and performance.
Own Wisconsin territory sales for XDEMVY, educating eye care customers, building account relationships, executing launch and growth plans, and driving compliant performance through data-informed selling.
Leads and develops a biopharma sales district, setting performance goals, coaching frontline representatives, building customer relationships, and aligning compliant execution to drive product launch and ongoing sales results.
Manage scientific relationships with eye-care KOLs, deliver disease-state education, gather insights to inform medical strategy, and support medical affairs initiatives across a designated territory.
Leads CMC planning and execution for drug substance development and manufacturing at CMOs, overseeing technical operations, supply strategies, regulatory submissions, budgets, and cross-functional program delivery.
Leads scientific strategy and execution for eyecare clinical studies, shaping development plans and trial designs while guiding cross-functional teams, interpreting data, and ensuring rigorous clinical and regulatory deliverables.
Leads global regulatory strategy for complex pharmaceutical products from early development through approval and lifecycle management, guiding submissions, health authority engagement, risk mitigation, and regulatory teams.
Own territory education, account development, and sales execution for an eye-care therapy launch, building customer relationships and using performance insights to grow product adoption while maintaining compliance.
Leads the East region’s Medical Science Liaison team, setting field medical strategy and developing scientific engagement with ophthalmology stakeholders while advancing medical affairs initiatives and cross-functional collaboration.
Leads analytical development for clinical-stage drug substance and drug product programs, advancing methods, control strategies, stability assessments, and CMC regulatory support through clinical and commercial milestones.
Provides strategic and hands-on leadership across clinical development, guiding trial design, execution, and data interpretation from first-in-human studies through registration while building a high-performing clinical organization.
Page 1 · 27 results
