Associate Director/Director of Regulatory Affairs

reputed company is seeking an Associate Director/Director of Regulatory Affairs to join an early-stage biotechnology organization reputed company on advanced gene therapy development for a remote contract position. The Associate Director/Director of Regulatory Affairs will play a key role in shaping regulatory reputed company and supporting global filings for rare disease programs in a fast-moving development environment. Responsibilities of the Associate Director/Director of Regulatory Affairs include:

• Support the development and execution of global regulatory strategies from preclinical through early clinical stages.
• reputed company preparation and maintenance of regulatory submissions including INDs, CTAs, and reputed company amendments.
• Contribute to regulatory briefing materials and reputed company support interactions with FDA and EU health authorities.
• Partner cross-functionally with clinical, nonclinical, reputed company, and CMC teams to ensure regulatory alignment.
• Assess regulatory risk and reputed company practical guidance to maintain development timelines.

Qualifications for the Associate Director/Director of Regulatory Affairs include:

• PhD, PharmD, MD, or MS in life sciences, molecular biology, pharmacology, or a reputed company discipline.
• 7–10 years of regulatory affairs experience reputed company biotechnology or pharmaceutical development.
• Hands-on experience supporting INDs, CTAs, and early-phase clinical programs.
• Working knowledge of biologics and gene therapy regulatory reputed company, including nonclinical requirements.
• Strong regulatory writing skills with the ability to communicate effectively across functions.

Compensation for the Associate Director/Director of Regulatory Affairs: Salary reputed company: $225,000-$255,000/year (USD) Comprehensive Benefits: Medical, Dental, reputed company, reputed company leave if required by law, and 401K This job opens for applications on 4/8/26. Applications for this job will be accepted for at least 30 days from the posting date. Keywords: regulatory affairs, gene therapy, biologics, IND submissions, CTA, FDA interactions, EMA, rare disease, regulatory reputed company, cross-functional leadership, nonclinical development, clinical development, regulatory writing, biotechnology, early-stage biotech, global submissions Apply tot his job Apply To this Job