Associate Director/Director, Regulatory Strategy

nChroma Bio is a clinical-stage genetic medicines company developing engineered epigenetic silencers to overcome the limitations of existing therapies and enable next-generation genomic medicines. By combining in vivo delivery and gene-regulating technologies, nChroma is designing optimal solutions to deliver precise, potent and durable treatments for patients with high unmet needs. nChroma’s lead candidate, CRMA-1001, is a clinical-stage, liver-directed epigenetic silencer in development as a potential functional cure for chronic hepatitis B. Guided by a world-class team at the forefront of genetic medicine, founded by renowned pioneers in the field, and supported by top-tier investors, nChroma is redefining targeted in vivo genetic medicine with the initial goal of treating diseases affecting the liver, blood, cardiovascular and central nervous systems. We’re building a culture and organization to support this important mission, bringing together individuals that thrive in a supportive environment where diverse perspectives and a passion for discovery drive cutting-edge science and breakthrough medicines. ABOUT THE ROLE  The Associate Director/Director, Regulatory Strategy will oversee the management, coordination and execution of regulatory activities for nChroma’s early development programs.  This position supports nChroma’s regulatory efforts and partners with the nonclinical, clinical development, and clinical operations functions, as well as other regulatory team members.  This role reports into the VP Regulatory Affairs.  RESPONSIBILITIES  Responsible for coordinating and driving regulatory submissions, including submission teams and timelines, for assigned programs  Represent regulatory function on cross-functional teams   Support US, EU, and global clinical trials including the preparation of initial INDs/CTAs and amendments, responses to agency questions, and maintenance activities.  Support development and implementation of regulatory strategies to facilitate the progress of programs through all phases of development  Collaborate with cross-functional teams to generate and refine the product development strategy  Ensure regulatory strategies align with business goals and meet Health Authority requirements.  Actively monitor regulatory policy and intelligence and disseminate information to teams; contribute to internal process and policy improvements.  SKILLS & COMPETENCIES:  Experience in gene therapy, gene editing and/or RNA therapeutics strongly preferred  In-depth knowledge of global regulations, ICH/GMP requirements, CTD format.  Thorough understanding of drug development process and the pharmaceutical industry including global regulatory requirements, guidance, accelerated regulatory review paths, and policy trends   Ability to work independently in a fast-paced environment   Ability to effectively collaborate in a dynamic, cross-functional environment to meet each program’s critical regulatory milestones   Excellent communication skills, regulatory writing skills and willingness to share knowledge and lessons learned with strong attention to detail   QUALIFICATIONS:  B.A. and/or M.S. with at least seven years of relevant experience within the biotech or pharmaceutical industry. Minimum of 5 years in regulatory affairs in a clinical-stage and/or commercial biotechnology company.  The salary range for this role is $180k - $235k nChroma Bio is an equal opportunity employer, providing equal opportunities to all employees and applicants for employment without regard to race, color, religion, sex or gender identity, national origin, age, disability, sexual orientation or genetics. In addition to federal law requirements, nChroma Bio complies with applicable state and local laws governing nondiscrimination in employment.  Offices: