Senior Director, Program & Portfolio Management

• Own the integrated Trutakna (atacicept-vymj) project plan and the full suite of supporting program management deliverables, timelines, milestones, dependencies, critical path, dashboards, and RAID logs, ensuring accuracy and decision-readiness at all times.
• Lead the Development Sub-Team, driving successful cross-functional execution of Trutakna development programs across Clinical Development, Regulatory Affairs, CMC, Biostatistics, Drug Safety, and other R&D functions.
• Lead Research and Development Governance, overseeing agenda development, meeting facilitation, decision tracking, and resolution of action items.
• Manage the weekly Development Sub-Team meeting end to end: build the agenda, produce meeting presentations, capture and distribute clear minutes, and drive closure on open items between meetings.
• Serve as a champion of PMO resources to direct reports and the broader organization. Lead with Program Management best practices, bringing rigor and discipline to teams and the PPM function..
• Serve as the principal execution partner to the Global Program Team Lead (GPTL) and GPT Program Manager, translating GPT-level strategy into coordinated execution plans and ensuring program risk and status are communicated clearly across governance layers.
• Partner closely with the Chief Medical Officer, Executive Vice President, Clinical Development and the Executive Vice President, Development Operations to keep clinical execution, timelines, and risk visibility tightly aligned with program governance and the RDRC.
• Manage and mentor a team of direct report program and/or project managers supporting R&D, fostering professional development and building program management capability across the team.
• Proactively identify and manage program risks and issues in partnership with functional leaders, escalating with clear options and recommendations when executive decisions are required.
• Maintain continuous, high-touch engagement with cross-functional stakeholders between formal governance touchpoints, ensuring alignment and swift resolution of emerging issues.
• Act as a trusted, credible partner to functional leaders and executive stakeholders, communicating program status, risks, and dependencies with clarity, precision, and professionalism.
• Continuously strengthen program management rigor and discipline within R&D, including governance cadence, reporting tools, and cross-functional communication norms.
• May support other programs or R&D initiatives as needed.

• BA/BS degree with 15+ years of biotechnology or pharmaceutical industry experience required; advanced degree (PhD, MD, MBA) preferred.
• Deep, hands-on experience managing late-stage development programs through registration and approval; direct BLA/NDA experience preferred.
• A blend of large biopharma and smaller, fast-moving biotech experience strongly preferred, combined with a high level of professionalism and experience working with executive leadership teams.
• Demonstrated experience leading cross-functional development sub-teams and running formal governance bodies at the program or portfolio level.
• Demonstrated people management skills, specifically managing program or project managers, required.
• Exceptional stakeholder management skills, with a proven ability to build trust and drive alignment with executive leaders and senior functional heads.
• Rigorous command of standard program management deliverables and disciplines, including integrated project plans, timelines, dashboards, and RAID logs.
• Excellent meeting management skills, including agenda design, facilitation, and producing clear, accurate, professional minutes and follow-up.
• Proven ability to operate as an execution owner, translating strategic direction set by others into a well-managed, on-track operating plan.
• High level of accuracy, attention to detail, and follow-through; comfortable managing significant offline stakeholder coordination between formal meetings.
• Ability to communicate effectively and with executive presence across the organization at all levels.
• Proven ability to manage competing priorities, timelines, and stakeholders in a fast-paced, rapid-growth environment.
• Experience with Smartsheet or similar project management tools preferred.
• PMP or equivalent certification a plus.
• Proficient in Microsoft Office, including Word, Excel, PowerPoint, Project, Visio, or other timeline tools.

Vera Therapeutics Inc. is an equal-opportunity employer.

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The exact base pay offered for this role will depend on various factors, including but not limited to the candidate’s geography, qualifications, skills, and experience.

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The successful candidate will be eligible for an annual performance incentive bonus, new hire equity, and ongoing performance-based equity.

Vera Therapeutics also offers various benefits offerings, including, but not limited to, medical, dental, and vision insurance, 401k match, flexible time off, and a number of paid holidays.

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