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Director, Regulatory Affairs - Infectious Disease Berkeley Heights, NJ

Remote / Online - Candidates ideally in
Berkeley Heights, Union County, New Jersey, 07922, USA
Listing for: Tonix Pharmaceuticals Holding Corp.
Remote/Work from Home position
Listed on 2026-03-15
Job specializations:
  • Healthcare
    Infectious Disease/ Epidemiology, Healthcare Management
Salary/Wage Range or Industry Benchmark: 100000 - 125000 USD Yearly USD 100000.00 125000.00 YEAR
Job Description & How to Apply Below
Director, Regulatory Affairs - Infectious Disease

About Tonix*

Tonix is a fully integrated biotechnology company, publicly traded on NASDAQ (ticker: TNXP), with marketed products and a pipeline of development candidates The Company is focused on commercializing, developing, discovering, and licensing therapeutics to treat and prevent human disease. In August 2025, Tonix received FDA approval for Tonmya™ (cyclobenzaprine HCl sublingual tablets), a first-in-class, once-daily, non-opioid treatment for fibromyalgia. Tonmya is the first new fibromyalgia therapy approved in over 15 years, following successful Phase 3 trials demonstrating significant symptom improvement.

Commercial launch is expected in the fourth quarter of 2025. Tonix also markets Zembrace® Sym Touch® (sumatriptan injection) 3 mg and Tosymra® (sumatriptan nasal spray) 10 mg, both indicated for the treatment of acute migraine with or without aura in adults.

Tonix’s development portfolio includes product candidates in central nervous system (CNS), immunology, immuno-oncology infectious disease and rare disease. The CNS pipeline features both small molecules and biologics to treat pain, neurologic, psychiatric, and addiction conditions. The immunology portfolio includes biologics to address organ transplant rejection, autoimmunity, and cancer. The infectious disease pipeline includes a vaccine in development to prevent smallpox and monkeypox, which also serves as a live virus vaccine platform for other infectious diseases.

Finally, therare disease portfolio includes a product in development for Prader-Willi syndrome, which has both orphan drug designation and rare pediatric disease designation grants from the FDA.

Tonix owns and operates a state-of-the art infectious disease research facility in Frederick, Md.

Please visit  for specifics on the pipeline.

* All of Tonix’s product candidates are investigational new drugs or biologics and have not been approved for any indication.

Position Overview

The Director, Regulatory Affairs for Infectious Diseases will serve as the primary Regulatory Lead for Tonix’s infectious disease biologics programs. This role oversees global regulatory strategy, submissions, health authority interactions, and cross‑functional leadership from early development (nonclinical, pre‑IND) through clinical stages. The ideal candidate is proactive, strategic, and comfortable operating with minimal oversight while driving timelines and influencing team direction. This position will report directly to the Head of Regulatory Affairs and will be based at a Tonix office or can be a remote-based position.

  • Serve as Regulatory Lead for biologics, focused on infectious diseases programs.
  • Develop and execute global regulatory strategies across nonclinical, CMC, and clinical development.
  • Lead preparation, authorship, and coordination of regulatory submissions, including pre‑IND packages, INDs, amendments, and briefing documents.
  • Direct interactions with FDA and other health authorities; prepare teams, lead discussions, and manage responses to queries.
  • Lead cross‑functional regulatory efforts by partnering with nonclinical, CMC, clinical, project management, and external partners/CROs.
  • Assess regulatory risks, impacts, and mitigation options; communicate recommendations to internal teams and senior leadership.
  • Ensure compliance with FDA, ICH, and global regulatory requirements, as well as internal SOPs and GxP standards.
  • Oversee regulatory documentation quality and timely delivery of program milestones.

Necessary Skills and Abilities

  • Strong scientific foundation in immunology, infectious diseases, or related biological disciplines.
  • Proven experience preparing and submitting INDs and related early‑phase regulatory documents.
  • Demonstrated ability to independently lead regulatory strategy and cross‑functional teams.
  • Strong knowledge of FDA, ICH, EU, and applicable global regulatory guidelines.
  • Excellent written and verbal communication skills, including regulatory writing and team communication.
  • Strong organizational, planning, and prioritization skills with high attention to detail.
  • Ability to manage multiple responsibilities in a fast‑paced,…
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