Executive Director Clinical Development Lead- Myasthenias Gravis

Executive Director Clinical Development Lead- Myasthenias Gravis

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 Sjgren's syndrome.

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

Position Overview

The Executive Director, Clinical Development Lead is responsible for driving the strategic and operational leadership of clinical development programs within Vor Bio. This role ensures the successful design, execution, and delivery of clinical trials, supporting the advancement of innovative therapies from late stage development through regulatory approval. The Executive Director will collaborate cross-functionally to shape clinical strategy, manage teams, and represent clinical development both internally and externally.

Key Responsibilities

Strategic Leadership :

• Develop and implement clinical development strategies for assigned programs, aligning with corporate objectives and regulatory requirements.
• Lead the planning and execution of clinical trials, ensuring scientific rigor and operational excellence.

Program Oversight :

Cross-Functional Collaboration :

Team Leadership :

Regulatory & Compliance :

Stakeholder Engagement :

Qualifications

Education :

Experience :

Skills & Competencies :

Why Join Vor Bio?

Impact : Play a pivotal role in advancing innovative therapies that improve patient outcomes.

Growth : Lead high-profile programs with opportunities for professional development and career advancement.

Collaboration : Work alongside passionate experts in a dynamic, mission-driven environment.

At Vor, we support our team with robust benefits, including comprehensive health coverage, flexible paid time off, generous parental leave, and a competitive 401(k). From education assistance to wellness resources and financial security, we invest in your well-being so you can thrive at work and beyond.

As an equal opportunity employer, we at Vor Bio know that diversity inspires innovation, inclusiveness, and creativity. We invite you to come as you are. All applicants will be considered for employment agnostic to race, age, color, religion, sex, sexual orientation, gender identity, national origin, veteran or disability status.