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Encoded Therapeutics

Precision gene therapies for pediatric CNS.

Associate Director, Development Program Manager

Program ManagementPosted on Nov 11
Full-timeRemote in USA

About the Job

Requirements

  • Typically requires a minimum of 8 years of related experience with a bachelor’s degree; or 6 years and a master’s degree; or a PhD with 3 years' experience; or equivalent experience.
  • Demonstrated experience in program or project management within the biotech, pharmaceutical, or related life sciences industry.
  • Working knowledge of the drug development process, including preclinical, clinical, regulatory, and commercial requirements.
  • Proven track record of successfully leading and managing cross-functional teams in the development and execution of complex development programs.
  • Strong organizational skills with the ability to manage a complex, multi-functional program.
  • Proficient in Smartsheet, Office Timelines, and/or other project management tools and software.
  • Proven ability to evaluate existing PMO tooling, workflows, and delivery frameworks; skilled at identifying operational bottlenecks and providing strategic recommendations to modernize and streamline processes.
  • Excellent written and oral communication skills, including experience preparing materials for and presenting to senior leadership.

Responsibilities

  • Facilitate development and implementation of program strategy, ensuring alignment with company goals, timelines, and budgetary constraints.
  • Organize Development Core Team activities that foster cross-functional collaboration, effective communication, and strategic discussion, ensuring stakeholders are aligned on program objectives and milestones to aid decision-making.
  • Ensure cross-functional teams are properly prepared for internal meetings, communications to management, and engagement with external partners.
  • Partner with the Director of PMO to ensure portfolio and cross-program considerations alignment.
  • Develop and maintain the integrated program plan, timeline, and budget across all functional areas for the assigned program.
  • Track deliverables resulting from Core Team meetings, ensuring timelines are met and objectives are achieved.
  • Identify program risks and dependencies early, and develop and track mitigation plans with functional leads, particularly for AAV gene therapy program considerations such as viral vector supply timelines, long-term follow-up requirements, and specialized dosing or delivery infrastructure for CNS administration.
  • Assist functional leads with implementing risk management strategies, proactively identifying and mitigating program risks and challenges.
  • Support scenario planning and contingency planning for key program decision points, such as go/no-go milestones, regulatory interactions, and data readouts.
  • Contribute to the development and refinement of program management processes, templates, and best practices across the organization.
  • Serve as the primary point of integration across functional areas for the program, ensuring consistent communication of program status, risks, and decisions.
  • Partner with functional leads to coordinate cross-functional projects related to CMC, Regulatory, Clinical, Medical, Patient Advocacy, and Nonclinical, providing support and guidance to achieve project goals.
  • Facilitate internal communication to identify risks and mitigations, escalating unresolved issues to the Director of PM as needed.
  • Partner with Finance and functional leads on budget forecasting.
  • Support resource planning and capacity analysis across functions to ensure the program is appropriately staffed.
  • Monitor and report program progress, providing regular updates to cross-functional teams, the PM Director, and other stakeholders, highlighting key achievements, challenges, and mitigation plans.
  • Utilize formal communication protocols and tools, including dashboards, reports, and weekly/monthly updates, to support company and operational goals.
  • Support maintenance of program documentation in alignment with internal quality and compliance standards.
  • Contribute to ad hoc functional projects across various departments.
  • Collaborate with team members to address challenges and find solutions for ad hoc projects, as needed.
  • Support Quarterly Business Review and Board of Directors meetings as needed.
  • Perform other duties as assigned.

Desired Qualifications

  • An advanced degree in life sciences, pharmacology, or a related field is preferred; an MBA or project management certification is a plus.
  • Experience supporting gene therapy, AAV vectors, or other advanced modality programs, and/or rare disease programs.
  • Experience supporting rare disease or CNS-focused gene therapy programs.
  • Familiarity with gene therapy-specific regulatory considerations.
  • Demonstrated experience leveraging AI-assisted features within modern program and portfolio management tools to automate workflows, synthesize project data, and enhance team productivity.
  • Experience with governance processes in a biotech or pharmaceutical organization, such as portfolio reviews and stage-gate processes.
  • Familiarity with IND submission.
  • Up to 20% travel may be required.

About the Company

Encoded Therapeutics

Precision gene therapies for pediatric CNS.

Encoded Therapeutics develops precision gene therapies for pediatric CNS disorders such as Dravet syndrome, using a targeting and regulation platform that directs genetic payloads to specific brain cell types based on genetic profiles. The approach aims to increase gene specificity, cell selectivity, and potency, while reducing off-target effects and toxicity. Therapies are designed to modify disease-causing genes in defined brain cells to provide lasting benefits. The company plans to translate these therapies into clinically effective treatments and commercialize them through partnerships with healthcare providers.

Company size
51-200
Company stage
Series F
Total funding
$514.1M
Headquarters
San Francisco, CA
Founded
2014

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