Director, Regulatory Affairs

AskBio Inc., a wholly owned and independently operated subsidiary of Bayer AG, is a fully integrated gene therapy company dedicated to developing life-saving medicines and changing lives. The company maintains a portfolio of clinical programs across a range of neuromuscular, central nervous system, cardiovascular, and metabolic disease indications with a clinical-stage pipeline that includes investigational therapeutics for congestive heart failure, limb-girdle muscular dystrophy, multiple system atrophy, Parkinson’s disease, and Pompe disease. AskBio’s gene therapy platform includes Pro10™, an industry-leading proprietary cell line manufacturing process, and an extensive array of capsids and promoters. With global headquarters in Research Triangle Park, North Carolina, and European headquarters in Edinburgh, Scotland, the company has generated hundreds of proprietary capsids and promoters, several of which have entered pre-clinical and clinical testing. Our vision: Pioneering science to create transformative molecular medicines. Our mission: Lead innovative science and drive clinical outcomes to transform people's lives. Our principles: Advance innovative science by pushing boundaries.  Bring transformative therapeutics to patients in need.   Provide an environment for employees to reach their fullest potential.   Our values: Be a Pioneer. We are not afraid of the impossible and to innovate to make gene therapies accessible to those in need. Cultivate Collaboration. Strive to be the best teammate, actively listen, openly communicate, and embrace diverse points of view. Embrace Responsibility. We are humbled by the enormity of our mission.  We hold a relentless commitment to advance science and clinical outcomes for our patients, families, and caregivers. Raise the Bar. Continuously drive improvements and efficiencies. Seek and provide constructive feedback. Have a bias for learning and action. Act with Uncompromising Integrity. Be honest, transparent, and committed to doing what’s right in every situation. Make clear commitments and follow through. Position Summary The Director, Regulatory Affairs will serve as a U.S.-based regulatory strategy lead for assigned development programs, with responsibility for driving global regulatory strategy and providing focused leadership for regulatory activities. This role will provide regulatory direction for preclinical and clinical development of AskBio’s product candidates, working closely with cross-functional Regulatory team members, Global Project Teams, subject matter experts, and external partners to ensure regulatory strategies are aligned with applicable health authority requirements and expectations. This position will support and/or lead interactions with global health authorities, including EMA and other European and ROW agencies, and will contribute to high-quality, timely regulatory submissions, agency meeting packages, regulatory designations, and development-stage submissions. The role will report into Regulatory Affairs and work remotely from within the United States. Job Responsibilities Serve as Regulatory Affairs lead or representative for assigned programs, providing strategic regulatory guidance and interpretation to support product development in alignment with applicable regulatory requirements and health authority expectations Develop and execute innovative, integrated regulatory strategies and timelines for assigned programs, including strategies that support global development and European regulatory objectives Lead or support preparation and submission of regulatory documents for clinical development programs, including CTAs, amendments, scientific advice briefing packages, regulatory designations, and future marketing application activities, as applicable Lead regulatory document review, comment resolution, and approval processes to ensure documents are high quality, scientifically sound, submission-ready, and aligned with regulatory strategy Prepare and/or contribute to health authority meeting requests, briefing documents, responses to questions, and other communications with regulatory authorities. Lead or participate in internal governance meetings, cross-functional project team discussions, and regulatory agency interactions, effectively communicating regulatory strategy, risks, options, and recommendations Collaborate closely with Clinical, Nonclinical, CMC, Quality, Medical, Project Management, and other functions to ensure regulatory strategies are appropriately integrated into development plans and executed in a timely manner Provide regulatory guidance on European requirements, expectations, procedures, and opportunities, including agency engagement and expedited development mechanisms where appropriate Manage or provide oversight of external regulatory partners, consultants, CROs, and vendors supporting assigned regulatory activities Support regulatory due diligence for busness development or licensing opportunities, as needed. Ensure regulatory activities are conducted in compliance with applicable regulations, guidelines, internal procedures, and quality standards by staying up to date on contemporary guidance, regulations and applicable directives and laws Demonstrate strong collaboration, accountability, sound judgment, and a patient-focused mindset in a fast-paced matrix environment Minimum Requirements Bachelor’s degree in a scientific, engineering, medical, pharmacy, or related discipline 10+ years of regulatory affairs or related drug development experience in the pharmaceutical, biotechnology, or related industry Experience supporting and/or leading regulatory submissions, health authority interactions, or regulatory strategy for clinical-stage development programs Experience with authoring and submitting PINDs, CTAs and INDs for biologics, gene therapy, cell therapy, or other advanced therapeutic technologies Demonstrated ability