[Hiring] Regulatory Affairs Manager, CMC & Clinical Development @Harrow, Inc.

Role Description

The Manager of Regulatory Affairs will develop and execute regulatory strategies across the product lifecycle, including early-stage development, IND submissions, clinical trial support, NDA filings, and post-approval CMC activities. This role will lead regulatory CMC strategy while also serving as a key regulatory partner to Clinical Development for IND preparation, clinical trial applications, FDA interactions, and lifecycle management.

The position collaborates cross-functionally with R&D, Clinical, Medical Affairs, Legal, QA, Manufacturing, and Commercial teams to ensure successful product development, regulatory approval, and compliance with FDA and global regulatory requirements.

Core Responsibilities

• Lead preparation, review, and submission of IND applications (including original INDs, amendments, annual reports, and safety updates)
• Develop a regulatory strategy to support clinical development plans, including Phase 1–3 trial progression
• Provide regulatory guidance for clinical protocol development and ensure alignment with FDA expectations
• Lead and support FDA interactions, including Pre-IND, End-of-Phase, and other Type B/C meetings
• Partner with Clinical and Medical teams to assess regulatory risk and develop mitigation strategies
• Ensure compliance with GCP and applicable clinical regulatory requirements
• Work closely with the executive leadership team to lead the development of regulatory strategies and objectives that result in successful registration and commercialization of Harrow’s ophthalmic products
• Oversee regulatory matters connected to INDs, NDAs, and OTC ophthalmic products
• As a regulatory product lead, ensure alignment of CMC, nonclinical, and clinical components to support successful IND, NDA, and post-approval submissions
• Independently define CMC content (data and documentation) requirements for regulatory submissions and review content for conformance with established requirements
• Plan and execute activities in support of INDs, NDAs, supplements, amendments, annual reports, and other regulatory submissions
• Review and assess change controls for regulatory impact and manage appropriate submission requirements
• Review and assess promotional materials for adherence to FDA guidance and current thinking
• Serve as a primary contact with the US FDA, fostering strong relationships and acting as an effective regulatory advocate for Harrow Health
• Provide regulatory guidance across all functional areas
• Develop robust regulatory structures, processes, and procedures based on expert understanding and industry insight
• Monitor the US regulatory landscape for changes affecting ophthalmic products and communicate impact to stakeholders

Qualifications

• BS/BA Degree in a Scientific Discipline, an advanced degree preferred
• 6+ years of pharmaceutical Regulatory Affairs experience, including:
• Direct experience authoring or leading IND submissions
• Regulatory support for clinical trial programs (Phase 1–3)
• CMC regulatory strategy and lifecycle management experience
• Demonstrated experience interacting with the FDA on clinical development programs
• Strong working knowledge of IND content requirements (Modules 2–5), ICH guidelines, and GCP regulations
• Experience preparing briefing documents and participating in FDA meetings (Pre-IND, Type B, etc.)
• Experience with NDA preparation and/or post-approval regulatory activities preferred
• Experience supporting early-phase drug development and first-in-human studies strongly preferred
• Ability to provide strategic regulatory guidance across development stages
• Strong problem-solving ability, attention to detail, flexibility, and teamwork orientation
• Excellent written and oral communication skills
• Active participation in Agency/Industry groups/forums preferred

Position Type

Remote

Travel

Up to 30%