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Tarsus Pharmaceuticals

Develops FDA-approved ophthalmic therapies

Senior Director - Clinical Sciences

Clinical Research OperationsConfirmed live in the last 24 hours
Full-timeIrvine, CA, USA

About the Job

Requirements

  • An advanced degree in sciences, such as a PharmD, MD, or PhD, and deep experience in early clinical development.
  • At least 10 years of biotech or pharmaceutical clinical development experience, including at least 8 years of leadership in clinical trial management.
  • A track record of people management, problem solving, collaboration, cross-functional leadership, and effective communication.
  • Expertise with standard operating procedures, Good Clinical Practice, and regulatory and compliance guidelines for clinical trials.
  • Willingness to be hands-on and work through details.

Responsibilities

  • Provide scientific leadership to cross-functional study and program teams, ensuring timely study start-up, enrollment, database lock, analysis, and readouts.
  • Lead the design of clinical development plans and individual study protocols, including objectives, endpoints, inclusion and exclusion criteria, assessments, and statistical assumptions.
  • Own clinical deliverables and contribute to protocol development, document authoring, data review, study-level problem solving, and execution decisions to ensure scientific rigor and operational excellence.
  • Shape clinical plans, including timelines, budgets, and oversight of clinical teams.
  • Build and maintain relationships with investigators, key opinion leaders, and external partners; contribute to publication strategy and scientific communications.
  • Drive innovation in clinical endpoints, biomarkers, and digital tools, and champion continuous improvement in clinical science processes, templates, and data review frameworks.
  • Author and critically review clinical and regulatory documents, including protocols, statistical analysis plans, clinical study reports, investigator brochures, and clinical value dossiers, ensuring scientific rigor, regulatory alignment, and quality execution.
  • Conduct research to develop foundational education material to inform early development program strategies.
  • Interpret clinical data and support data-driven decisions.
  • Serve as program lead on early development core teams, investigator meetings, and scientific advisory boards.
  • Engage with internal and external stakeholders, including key opinion leaders and regulators.
  • Foster an innovative mindset, business acumen, outcome-driven orientation, and commitment to growing the team's capabilities and capacity.
  • Collaborate with Clinical Operations, Regulatory Affairs, Translational Sciences, Biostatistics, Medical Affairs, and others to ensure robust trial design, scientific and operational alignment, and execution.

Desired Qualifications

  • Experience in ophthalmology is preferred; experience in dermatology or infectious diseases is a plus.

About the Company

Tarsus Pharmaceuticals

Develops FDA-approved ophthalmic therapies

Tarsus Pharmaceuticals develops and markets treatments for eye care and infectious diseases, including XDEMVY (lotilaner ophthalmic solution 0.25%), an FDA-approved eye drop for Demodex Blepharitis. The product is applied as a medicated eye drop to kill Demodex mites and relieve eyelid inflammation. The company differentiates itself with a focused ocular/infectious-disease portfolio, an FDA-approved therapy, and active partnerships to expand its research and reach. Its goal is to address unmet medical needs, grow its product lineup through commercialization, and pursue new indications in eye care and infectious diseases.

Company size
201-500
Company stage
IPO
Headquarters
Irvine, CA
Founded
2017

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