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Tarsus Pharmaceuticals

Develops FDA-approved ophthalmic therapies

Manager 2 - Program Management, Late-Stage Development

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

About the Job

Requirements

  • At least 8 years of product development experience in biotech or pharmaceutical settings, including at least 5 years in a project or program management role.
  • Experience managing drug development programs from preclinical through Phase III studies.
  • A bachelor's degree in a biopharmaceutical-related field, such as biology, chemistry, or engineering.
  • Working knowledge of the end-to-end drug development process, including GxP/ICH guidelines and health authority interactions, for late-stage programs.
  • Ability to pivot effectively in response to changing priorities across programs and resources.
  • Proficiency with IT and project management tools such as Outlook, Excel, PowerPoint, MS Project, Smartsheet, or similar.
  • Established track record of people management, problem solving, collaboration, cross-functional leadership, and communication.
  • Strong communication, influencing, stakeholder management, and decision-making skills.
  • Strong project/program management foundation.
  • Excellent communication and emotional intelligence to lead cross-functional stakeholders in achieving deliverables on time and within budget, with the ability to implement effective processes and innovative solutions that improve program management efficiency.
  • Ability to identify, analyze, and resolve issues or challenges effectively and efficiently; demonstrate creativity, decisiveness, and capacity to implement structured, outcome-oriented solutions; navigate uncertainty without an established blueprint; and take ownership of decisions and actions.
  • Ability to build strong relationships and networks; respect differing points of view; cultivate a safe space for discussion and debate; and prioritize the team.
  • Ability to define mutual expectations, adapt to changing business needs, find solutions despite obstacles, and take appropriate actions, including calculated risks, to meet obligations.

Responsibilities

  • Partner with the Program Team Lead and Development Core Team to develop and execute cross-functional program strategy and integrated development plans for a late-stage program.
  • Establish and maintain integrated program timelines across clinical, regulatory, CMC/manufacturing, quality, nonclinical, medical affairs, and commercial activities to support program analyses, identify critical-path activities, and surface resource constraints.
  • Lead cross-functional planning and coordination for pivotal Phase 3 trial execution, database lock, and topline readout activities.
  • Drive integrated regulatory submission planning and execution, such as NDA/BLA/MAA submissions, with Regulatory Affairs and align cross-functional deliverables to support timely, high-quality filings.
  • Support launch-readiness planning by coordinating clinical development, regulatory, medical affairs, commercial, and supply chain/manufacturing activities.
  • Identify and assess program risks; develop, track, and drive mitigation and contingency plans, including maintaining a program risk register.
  • Lead scenario planning to prepare teams for differing outcomes at key milestones, including pivotal readouts, regulatory interactions, and launch.
  • Challenge assumptions and recommend improvements to program processes, decision-making, and outcomes.
  • Facilitate and document Development Core Team and sub-team meetings, cross-functional communications, and governance decisions, ensuring alignment with internal functional groups and leadership.
  • Support program budget and resource planning with Finance and functional leads, track spending against forecast, and flag variances.
  • Build relationships with key functional stakeholders and their leaders across the organization to support program goals.
  • Serve as a Program Management subject matter expert and resource for the broader organization, championing program management best practices and continuous improvement.

Desired Qualifications

  • Direct experience supporting a program through pivotal trials, regulatory submission, and launch readiness is strongly preferred.
  • PMP or PgMP certification is preferred but not required.

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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