Associate Director, Regulatory Science

About this role

Location: Remote
Reporting to: Executive Director, Regulatory Science

Orchard Therapeutics, a Kyowa Kirin company, is a global gene therapy leader focused on transforming the lives of patients with rare disorders through innovative gene therapies based on gene-modified hematopoietic stem cells (HSCs). Orchard has its global headquarters in London, England, and its U.S. headquarters in Boston, Massachusetts.

Job Summary
This role is a unique opportunity to join the Regulatory Science team, which is responsible for the development of global regulatory strategy and execution of regulatory activities for ex-vivo Gene Therapy assets. This role reports to the Executive Director, Regulatory Science located in the US. This position is unique and ideal for someone with a solid US regulatory background who can develop innovative regulatory strategies and apply strong skills in execution, collaboration, problem-solving, and attention to detail to contribute to groundbreaking science.

Key Responsibilities
Act as US regulatory lead on assigned program(s)
Work in close partnership with the Global Regulatory Lead(s) and under the oversight of the Executive Director, Regulatory Science to provide necessary regulatory inputs to the related cross-functional program teams
Develop the US regulatory strategy under the oversight of the Executive Director, Regulatory Science, including any innovative procedures to expedite the path to approval, in line with corporate goals, in partnership with the Global Regulatory Lead(s) and the program regulatory team(s)
Help identify regulatory risks, develop mitigation strategies, and support proactive agency engagement plans.
Support integrated regulatory planning across clinical, nonclinical and chemistry and manufacturing,
Execute the US regulatory strategy:
Be the primary liaison with US regulatory authorities for the assigned program(s)
Plan, prepare, and review submissions to the FDA, including Orphan designation applications (ODD), Investigational New Drug (IND) applications, Fast Track/RMAT designations, and Pediatric study plans
Prepare FDA meeting requests, briefing documents, coordinate and prepare cross-functional teams for meetings, and interface with US regulatory authorities
Coordinate and prepare responses to questions and requests for information from US regulatory authorities
Ensure that regulatory documents are accurate, complete, compliant with applicable regulatory requirements and prepared in accordance with the defined timelines
Actively participate in regulatory compliance and regulatory team development:
Monitor, analyze, and disseminate intelligence on US regulatory matters that may affect ongoing development programs
Lead the implementation of new US regulations/guidelines applicable and relevant to development programs in close collaboration with the Global Regulatory Lead(s) and relevant functional leads
Contribute to updates, improvements and development of processes (including new SOPs as applicable) linked to regulatory activities
Participate in internal audits and future HA inspections
Share expertise and learning experiences - “grow together” approach within the regulatory team.
Requirements
Required Knowledge/Experience
Significant experience in the development and execution of US regulatory strategies for development programs in industry‑related US Regulatory Affairs
Knowledge and experience of development/registration of biologics and/or Advanced Therapy Medicinal Products (ATMPs) is a plus
Very good knowledge and understanding of US CFR and FDA guidelines is a must – understanding of EMA regulations and guidelines is a plus
Previous experience in using US innovative expedited paths to approval in the frame of global development is a plus
Track record of INDs preparation, management up to FDA clearance and maintenance
Previous experience of leading a team to prepare for and attend major health authority interactions (e.g., pre-IND meeting, EOP1, EOP2 meetings, etc.)
Experience in regulatory submission project management
Previous experience in the preparation and submission of a BLA is a plus
Education / Key Competencies
PharmD or PhD in a scientific discipline.
Regulatory Affairs certification is a plus
Strong attention to detail, translating into the ability to produce high-quality regulatory documents.
Ability to establish and maintain a positive, strong and efficient collaborative working relationship within the Regulatory team and with other functions and stakeholders
Ability to handle multiple tasks in parallel in a fast-paced environment; ability to plan, prioritize and respond effectively to program/activities changes.
Ability to develop partnerships that support a strong cross-functional and inclusive team environment
Ability to work in autonomy on allocated program(s)
Excellent organizational, computer and documentation skills.
Solution-oriented approach to problem-solving including assessing variables, evaluating fundamental issues, anticipating business impact and providing direction.
General interest in a broad range of Regulatory activities.
Strong interpersonal skills including verbal and written communication.

Salary Range:

The anticipated salary for this position will be $190,000 - $240,000.  The actual salary offered for this role at commencement of employment may vary based on several factors including but not limited to relevant experience, skill set, qualifications, education (including applicable licenses and certifications), job-based knowledge, location, and other business and organizational needs. The company may ultimately pay more or less than the posted range. The listed salary is just one component of the overall compensation package. At Orchard Therapeutics North America we provide a comprehensive range of benefits in addition to incentive programs.

The compensation and benefits information set forth in this posting applies to candidates hired in the United States – and this range is specific to…