Director, Regulatory Affairs

Pelthos•Durham, NC

About The Position

Pelthos Therapeutics is a bio-pharmaceutical company committed to commercializing innovative, safe and efficacious therapeutic products to help patients with unmet treatment burdens. The Director, Regulatory Affairs develops, implements, leads and supports regulatory strategies for assigned projects in collaboration with various cross-functional teams. The Director, Regulatory Affairs will execute developed strategies for earliest possible approvals of the company’s regulatory applications at all stages of product development and post approval activities. They will facilitate publishing activities with internal and external stakeholders including authoring cover letters forms, eCTD sections and preparing documents for submission to regulatory agencies, as well as ensuring that they meet current regulatory requirements and industry standards, are high quality, consistent, and complete.

Requirements

MS or advanced level degree in either chemistry, biological or biomedical related fields.
10+ years demonstrated experience in drug regulatory affairs in the pharmaceutical or biotech industry.
In depth knowledge of FDA regulatory requirements with hands on experience interacting directly with the Food and Drug Administration.
Ability to think strategically, operationally and tactically to bring regulatory insight to pre-approval and post-approval activities.
Experience in guiding an organization around filing strategies.
Demonstrated background in coordinating across disciplines to ensure timely filings.
Hands-on experience with INDs, and NDAs filing requirements.
Ability to work collaboratively as the regulatory affairs business partner to local development and commercialization teams.
Sound judgement and ability to analyze situations and information.
Makes decisions based on facts and figures rather than on assumptions.
Ability to develop an in-depth understanding of milestones and associated implementation timelines for regulatory interactions, strategies, and key decisions points to support existing and future development activities.
Strong organization and planning skills.

Nice To Haves

Experience with the Dermatology and Dental Product Division and/or the Division of Anti-Infectives of the FDA and other regulatory regions and agencies would be an asset including understanding of other medicinal products such as medical device requirements.

Responsibilities

Content Management Responsible for content management and integration of content assembled from cross-functional subject matter experts to support document finalization and publishing.
Project Management Ability to develop and execute regulatory strategies for drug development, registration, and post-marketing activities.
Assist with the planning, coordination and management of internal regulatory preparatory meetings and the preparation of staff members participating in these meetings that will support formal regulatory interactions.
Leads the Regulatory Affairs functional responsibilities in Change Management Activities.
Assures regulatory compliance with safety reporting, IND/NDA updates and accessibility to historic documentation required to maintain compliant activities across the organization.
Serves as the primary contact for all interactions with regulatory agencies such as the FDA.
Oversee document publishing and management of publishing vendor for regulatory submissions.
Responsible for supporting the creation and management of submission plans and ensure coordination of development/commercial activities with the submission processes to drive agreed-upon timelines.
Identify process improvement for internal systems and processes related to publications, submissions and archiving of regulatory records.
Monitor and assess changes in regulatory requirements, guidelines, and legislation, and provide guidance to internal stakeholders on potential implications and opportunities for the business.
Complete other duties as assigned