Associate Director, Program Management

Vera Therapeutics (Nasdaq: VERA), is a late clinical-stage biotechnology company focused on developing treatments for serious immunological diseases. Vera’s mission is to advance treatments that target the source of immunologic diseases in order to change the standard of care for patients. Vera’s lead product candidate is atacicept, a fusion protein self-administered at home as a subcutaneous once weekly injection that blocks both B-cell Activating Factor (BAFF) and A Proliferation Inducing Ligand (APRIL), which stimulate B cells to produce autoantibodies contributing to certain autoimmune diseases, including IgA nephropathy. Vera is also evaluating the role of atacicept in other immunologic disorders. Additionally, Vera is developing VT-109, a novel, next-generation dual BAFF/APRIL inhibitor in preclinical development, and MAU868, a monoclonal antibody designed to neutralize infection with BK virus, a polyomavirus that can have devastating consequences in certain settings such as kidney transplant. For more information, please visit: www.veratx.com.

Our values are the cornerstone of our culture. Our values inspire us every day and guide everything we do—from how we hire great people, to advancing our mission together, to achieving our ultimate goal to improve medical treatment for patients suffering from immunological diseases.

Position Summary:

We are seeking a highly skilled and motivated Associate Director, Program Management reporting to the Senior Director, Program Management. The ideal candidate will manage the planning and execution of our lead late-stage development Program, Atacicept, in alignment with Vera’s Regulatory strategy and our commitment to health authorities globally.

Responsibilities:

• Develop and execute comprehensive regulatory plans, timelines, and budgets for Atacicept while ensuring Regulatory alignment with organizational objectives.
• Act as liaison between Regulatory and other Development functions; gathering and disseminating key decisions and updates across cross-functional workstreams and activities.
• Providing Regulatory Submission Program Management support including timeline development, issue and risk management, status reporting and meeting facilitation both generally and for specific modules.
• Work with other program managers to integrate module timelines and deliverables into the overall Regulatory Submission plans.
• Collaborate with Regulatory and cross functional stakeholders to manage timeline for submission documents, including IB, DSUR, PSUR, ODD annual updates, and annual reports.
• Support development and maintenance of the Smartsheet environment necessary to manage Regulatory filings, including creating/maintaining templates and dashboards, setting up automation and transferring existing plans.
• Provide program management support for briefing documents and agency meetings.
• Coordinate submission scheduling with regulatory publishing and ensure delivery of high-quality documents.
• May support other programs.

Qualifications:

• BA/BS degree with 8+ years of biotechnology industry experience required.
• In-depth knowledge of some aspects of the biopharmaceutical industry, biologic development is preferred.
• Experience in Regulatory and global filings required.
• High level of accuracy and attention to detail.
• Ability to work with ambiguity, and create new, more efficient processes; desire to bring order and organization to a newly developing organization.
• Ability to communicate effectively with stakeholders across the organization at all levels.
• Proven ability to manage competing priorities, budgets, and timelines in a fast-paced, rapid-growth environment.
• Highly skilled at working collaboratively with cross-functional teams and contractors to drive results and meet company objectives.
• Ability to distill, organize, and effectively communicate (verbal and written) key messages from complex discussions.
• Self-directed and proactive with ability to function independently in certain situations, exercise good judgment and respond quickly and effectively to changing environments.
• Ability to deal with uncertainty and unanticipated challenges in a constructive manner and generate options for moving forward.
• Demonstrated people management skills, specifically managing other program managers.
• Experience in Smartsheet is preferred but not required.
• Proficient in Microsoft Office, including Word, Excel, Project, Visio, or other timeline tools.

Vera Therapeutics Inc. is an equal-opportunity employer.

Vera Therapeutics is committed to fair and equitable compensation practices and we strive to provide employees with total compensation packages that are market competitive. For this role, the anticipated base pay range is $ - $. 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.

At Vera, base pay is only one part of your total compensation package. 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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We require that all recruiters and staffing agencies have a fully executed, formal written agreement on file.

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