Join us in tackling autoimmune disease at its root. At Vor, we believe science can change the course of disease, not just manage symptoms. 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, rewriting what is possible for patients worldwide.

Impact & Growth

Contribute directly to a medicine with best‑in‑disease Phase 3 results in myasthenia gravis and expansion into multiple autoimmune diseases. Be part of a rapidly scaling company offering career growth in science, clinical development, commercial strategy, and beyond.

Key Responsibilities

• Lead and manage the biometrics function, including biostatistics, data management, and statistical programming teams.
• Develop and implement biometrics strategies to support clinical development plans, regulatory submissions, and post‑marketing activities.
• Oversee design, analysis, and interpretation of clinical trials, ensuring statistical rigor and compliance with regulatory standards.
• Establish and maintain best practices for data collection, management, and analysis, ensuring data integrity and quality.
• Collaborate with cross‑functional teams (clinical, regulatory, medical, and project management) to align biometrics deliverables with program objectives.
• Provide expert guidance on statistical methodologies, protocol development, and study design.
• Represent biometrics in interactions with regulatory agencies, external partners, and key stakeholders.
• Mentor and develop biometrics staff, fostering a culture of excellence, innovation, and continuous improvement.
• Monitor industry trends and emerging technologies to enhance biometrics capabilities and processes.

Qualifications

• Advanced degree (PhD or MS) in Biostatistics, Statistics, Mathematics, or related field.
• 10+ years in biometrics leadership roles within pharmaceutical, biotechnology, or CRO industry.
• Proven track record in designing and analyzing clinical trials (Phase I‑IV) and regulatory submissions (NDA/BLA/MAA).
• Expert knowledge of statistical software (e.g., SAS, R) and clinical data management systems.
• Strong understanding of global regulatory requirements (FDA, EMA, ICH guidelines).
• Exceptional leadership, communication, and organizational skills.
• Ability to work collaboratively in a fast‑paced, matrixed environment.

Core Competencies

• Strategic Thinking – set vision and direction for biometrics functions.
• Technical Expertise – deep understanding of statistical methodologies and clinical data standards.
• Collaboration – build relationships across disciplines and drive cross‑functional initiatives.
• Problem Solving – proactively identify challenges and implement effective solutions.
• People Development – mentor and grow high‑performing teams.

Benefits

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, Vor Bio hires based on qualifications, experience, training, and ability to perform required job functions. We do not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or veteran status.