Senior Data Manager

🏢 Vorbiopharma · 📍 Boston, MA 💰 $170,000 - $170,000 / 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.

 

Location: Boston, MA preferred

The Senior Data Manager is responsible for all data management activities from study start-up through database lock and archiving and independently supporting the needs of the clinical study and programs of studies.  The Senior Data Manager will ensure completeness, accuracy and consistency and meet the standards of quality analysis and reporting to regulatory bodies.  In addition, the Senior Data Manager has an active role in continuous improvement and acts as a leader in the department as demonstrated by successful mentoring and consistent study delivery over time. 
 
Responsibilities: 
 

🎯 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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