Associate Director, CMC Program Management New

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:

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 of CMC Program Management reporting to the Senior Director, CMC Program Management. The ideal candidate will partner with the Vice President, Manufacturing Operations to oversee and execute on CMC commercial, lifecycle management, and preclinical activities at Vera. The successful candidate will be detail-oriented, self-directed, flexible, and able to manage the workload to meet programmatic milestones.

Responsibilities:

• Develop, maintain, and track project timelines and deliverables for CMC activities, ensuring alignment with organizational and departmental objectives.
• Coordinate commercial supply readiness and next generation process development activities across CMC, quality, regulatory, commercial, and external CDMO/CMOs.
• Act as a liaison between CMC team and external partners, consolidate and disseminate key decisions and updates across cross-functional workstreams.
• Support CMC Subteam and other governance forums to develop, track and execute on CMC functional objectives and lifecycle management initiatives.
• Work with CMC team to develop, manage and track the CMC budget.
• Provide CMC project management support, both internally and externally with vendors. This includes activities such as drug substance/drug product development, manufacturing, and supply chain oversight. Proactively track and manage activities at vendors and facilitate resolution of issues to keep project activities on track.
• Create and maintain program management tools to communicate timelines, deliverables, issues, risks, and mitigations. Ensure cross functional alignment on program status including expectations, opportunities, and risks.

Qualifications:

• BS/MS degree in a scientific or engineering discipline. PMP is a plus.
• 8 years of biotech experience in any of the following sub-disciplines; process development, manufacturing, and/or analytical development.
• 5 years of CMC program management experience.
• Proficient in Microsoft Project.
• Experience in Smartsheet is preferred but not required
• High level of 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.
• Excellent written and verbal communication skills, including a demonstrated ability to effectively communicate in a program team environment, within department, among functional groups, and external collaborators.
• Self-directed and proactive with ability to function independently, exercise good judgment, and respond quickly and effectively to changing environments.

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. 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.

For this role, the anticipated base pay range is

$148,000 - $226,000 USD

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