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Tarsus Pharmaceuticals

Develops FDA-approved ophthalmic therapies

Senior Director - Regulatory Affairs Strategy

Regulatory & Quality (Life Sciences)Confirmed live in the last 24 hours
Full-timeRemote in USA

About the Job

Requirements

  • At least 15 years of regulatory affairs experience in US and ex-US environments.
  • A higher degree (MS, Ph.D., or PharmD) in a scientific discipline.
  • Excellent verbal and written communication skills.
  • Critical thinking, leadership, assertiveness, negotiation, and project management skills evidenced by past performance on drug development project teams.
  • Ability to function at a high level in a team setting or as an individual contributor.
  • Understanding of US FDA and international pharmaceutical guidance, regulations, drug development processes, and industry standard practices.
  • Attention to detail and ability to coordinate and prioritize assigned projects.
  • Ability to make decisions by applying structured analysis to complex challenges, balancing competing priorities and long-term impacts, engaging stakeholders, and driving solutions aligned with organizational goals.
  • Ability to promote collaboration by aligning diverse teams around shared goals, fostering healthy debate, and building networks that strengthen organizational effectiveness and cross-team learning.
  • Ability to align teams around shared priorities, address risks and dependencies, and drive cross-functional accountability to deliver results.
  • Business acumen to anticipate market dynamics and use financial and strategic insight to guide investments, manage risk, and align priorities with long-term organizational value.
  • Ability to champion new ideas, invest in enabling systems and partnerships, and translate innovation into sustainable growth and organizational resilience.

Responsibilities

  • Guide assigned projects throughout development and lifecycle management by providing regulatory thought leadership and leveraging extensive development experience.
  • Provide strategic and tactical regulatory leadership across all phases of product development, filing, and lifecycle management to support timely approval and compliant post-market performance in the US and key international markets.
  • Anticipate and mitigate regulatory risk, ensure compliance with global regulatory requirements, and develop development-acceleration strategies.
  • Collaborate across organizational levels and functions, engage stakeholders, and influence cross-functional decision-making to drive regulatory success.
  • Oversee development and execution of global regulatory strategies from early development through post-approval for complex assets and indications, partnering with regulatory strategists and cross-functional stakeholders.
  • Provide regulatory leadership in global regulatory and product teams, including development regulatory strategy, planning, preparation, and execution of major US and global regulatory submissions, global submission rollout, and lifecycle management strategies for marketed products and post-approval changes.
  • Represent Regulatory Affairs in governance and interactions with global health authorities, as applicable, to enable efficient pathways from development through lifecycle management.
  • Be accountable for all US regulatory submissions and approvals for assigned projects.
  • Identify and communicate regulatory hurdles, risks, opportunities, and innovative pathways to accelerate development and approval.
  • Develop and lead regulatory intelligence gathering and regulatory influence management at the portfolio level.
  • Provide strategic leadership and development to other regulatory strategists to ensure innovative, robust, fit-for-phase regulatory strategies from first-in-human through approval.
  • Provide regulatory strategy leadership for business development and due diligence, including asset assessment, risk identification and mitigation, precedent leverage, and regulatory probability of success.
  • Establish best practices across Regulatory Affairs and other R&D functions to support consistent, high-quality execution.
  • Follow company policies and procedures for regulatory record keeping and lead development of new regulatory policies and procedures.
  • Advance organizational goals by participating in and taking leadership roles in professional associations, industry, and trade groups as appropriate for assigned projects.
  • Coordinate and prioritize assigned projects.
  • Travel up to 20% as 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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