
Senior Program Manager, Plasmid DNA / Cell and Gene Therapies
Posted 4 days ago

Posted 4 days ago
This is a fully remote position, open to applicants in California, +6 more states.
• Oversee highly intricate, multi-program portfolios for strategic accounts.
• Manage comprehensive delivery across multiple simultaneous projects with considerable revenue, risk, and inter-departmental dependencies.
• Ensure compliance with timelines, budgets, and key performance indicators (KPIs).
• Cultivate and influence senior-level client relationships and account strategies.
• Serve as a trusted advisor to client stakeholders, manage escalations, and shape program direction and long-term partnership outcomes.
• Facilitate enterprise-wide alignment and decision-making among cross-functional teams and leadership levels.
• Establish and uphold program governance frameworks.
• Monitor project metrics and predict capacity needs.
• Provide consistent updates to senior leadership on project status, risks, and opportunities.
• Convert master service agreements, statements of work, supply and quality agreements, amendments, and change orders into actionable operational requirements.
• Collaborate with Business Development, Legal, Contracts, and Finance to assess feasibility, manage scope changes, support negotiations, and safeguard Aldevron's commercial and contractual interests.
• Maintain overall program health and capacity strategy.
• Anticipate demand, identify risks, lead proposals and renewals, and drive account expansion and continuous improvement initiatives.
• Work in conjunction with Business Development, Legal, Contracts, Project Management, Manufacturing, Quality, Regulatory Affairs, Supply Chain, Technical Operations, Finance, and Executive Leadership.
• A Bachelor’s degree (B.S. or B.A.) is required.
• At least 7 years of experience in a client-facing role as a project, program, or account manager in the life sciences sector is preferred.
• Minimum of 5 years in a GMP-regulated CDMO setting is preferred.
• Proven experience managing programs and contracts in a regulated biotechnology, pharmaceutical, or medical device-related field is required.
• Familiarity with plasmid DNA manufacturing and its applications in cell and gene therapy, gene editing, mRNA, vaccines, or other genomic medicine is essential.
• Strong preference for experience with late phase/commercial drug products.
• Excellent analytical and problem-solving capabilities.
• Willingness to travel up to 25% of the time, including to the Fargo, ND site and client locations, with overnight travel as necessary based on business and customer requirements.
• An advanced degree in a scientific field is strongly preferred.
• An advanced degree in a scientific, engineering, legal, project management, or business discipline, or a project management certification such as PMP is a plus.
• Direct program leadership experience for commercial or late-phase plasmid DNA programs is a plus.
• Experience managing strategic accounts, cross-site programs, long-term supply agreements, capacity reservation models, demand planning, forecast commitments, pricing protections, change-order mechanisms, termination provisions, executive governance, or commercial supply continuity is a plus.
• Bonus/incentive compensation.
• Paid time off.
• Medical insurance.
• Dental insurance.
• Vision insurance.
• 401(k) plan.
• Remote work arrangement from home.
• Flexible remote working arrangements for eligible positions.
• Reasonable accommodations for applicants and employees with disabilities.
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