
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 Sjögren’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:
- Oversee late phase clinical development, from protocol design to study completion and data analysis.
- Manage timelines, budgets, and resources to ensure efficient program delivery.
- Cross-Functional Collaboration:
- Partner with Regulatory Affairs, Medical Affairs, Biostatistics, Data Management, and other key stakeholders to ensure integrated program execution.
- Facilitate communication between internal teams and external partners, including CROs, investigators, and regulatory agencies.
- Team Leadership:
- Build, mentor, and lead high-performing clinical development teams.
- Foster a culture of innovation, accountability, and continuous improvement.
- Regulatory & Compliance:
- Ensure all clinical activities comply with GCP, ICH guidelines, and applicable regulations.
- Prepare and present clinical data and program updates to regulatory authorities and advisory boards.
- Stakeholder Engagement:
- Represent Vor Bio at scientific conferences, advisory meetings, and industry forums.
- Engage with key opinion leaders and external experts to inform clinical strategy.
Qualifications
- Education:
- Advanced degree (MD, PhD, PharmD, or equivalent) in a relevant scientific discipline.
- Experience:
- Minimum of 15+ years in clinical development within the pharmaceutical or biotechnology industry.
- Proven track record of leading successful clinical programs and cross-functional teams.
- Experience with regulatory submissions and interactions.
- Skills & Competencies:
- Strong strategic thinking and problem-solving abilities.
- Excellent communication, presentation, and interpersonal skills.
- Ability to manage multiple priorities in a fast-paced environment.
- Demonstrated leadership and team-building capabilities.
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.
Please visit our website at https://www.vorbio.com/ for more information.
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