Senior Manager Statistical Programming

🏢 Vorbiopharma · 📍 Boston, MA 💰 $190,000 - $190,000 / yr

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Position Summary & Responsibilities

Join Us in Tackling Autoimmune Disease at Its Root

At Vor, we believe science can do more than manage symptoms. It can change the course of disease. By advancing telitacicept, a first- and potentially best-in-class dual BAFF/APRIL inhibitor, we are silencing upstream survival signals and stopping downstream autoimmune cascades. Together, we are addressing disease at its root cause and rewriting what is possible for patients worldwide.

When you join Vor, you’re not just working on a medicine. You’re part of a mission to redefine the future of autoimmune care.

Why Work at Vor?

Impact: Contribute directly to a medicine with best-in-disease Phase 3 results in myasthenia gravis and expansion into multiple autoimmune diseases.

Growth: Be part of a rapidly scaling company with opportunities to grow your career in science, clinical development, commercial strategy, and beyond.

Innovation: Work on a platform with potential beyond one indication — a therapy that has already shown consistent results across lupus, IgA nephropathy, and Sjögren’s syndrome.

Belonging: Join a culture where every voice is heard, and where our shared mission unites us across functions and geographies.

Senior Manager, Statistical Programming

Position Summary

The Senior Manager, Statistical Programming will provide hands-on statistical programming leadership and support for assigned clinical studies and collaborate with Biostatistics, Clinical Data Management, Clinical Operations, Safety, and other study functions. This role is responsible for the design, development, validation, and quality control of SAS programs used to access, transform, analyze, report, and submit clinical trial data.

The Senior Manager will serve as lead programmer for assigned studies, provide technical guidance to project te

🎯 Candidate Preparation Guide For Vorbiopharma Applicants

Key Role Competencies & Evaluation Highlights

Key Role Focus:

Evaluating pioneering cell and gene therapy execution with stringent adherence to cellular engineering protocols.

📋 Preparation Priorities (Key Areas to Clarify):

1. Lax attitude toward regulatory compliance or CMC (Chemistry, Manufacturing, and Controls)
2. Treating cellular therapies like traditional small-molecule pharma
3. Inability to manage multi-variable biological data sets

✨ Recommended Role Alignment Hook:

I combine precise cellular engineering with translational rigor to advance next-generation hematopoietic stem cell therapies.

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