Associate Director, Statistical Programing

Associate Director, Statistical Programmer

J oin 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.

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.

Responsibilities

• Serve as a lead study programmer to support activities including review of SAP, set‑up of mock TFL, dry run, draft and final TFLs.
• Collaborate with other functions for requirements such as safety updates, publications, etc.
• Effectively design and develop SAS programs, including micros for efficiency and consistency.
• Participate in standardization and process improvement initiatives.
• Support FDA submission as needed.
• Code complex SAS programs (including Macro language, SAS / STAT and SAS / GRAPH) for applications designed to analyze and report complex clinical trial data and for electronic review, exchange, transformation, and submission of data in CDISC SDTM format; consistently meeting study objectives.
• Perform quality control checks of SAS code and output produced by other Statistical Programmers.
• Demonstrate proficient knowledge of clinical development and medical data.
• Solve clinical trial reporting problems and provide proven technical proficiency in supporting daily operations and ensuring that project tasks are completed accurately with limited supervision.
• Create CDISC data sets by transforming various raw data sources, including different Electronic Data Capture (EDC) databases and Interactive Web Response Systems (IWRS), tables, figures, and listings, reporting and submitting the results of clinical trials for investigational medications.
• Work with all types of coding dictionaries (MedDRA and WHODD) commonly used by the pharmaceutical industry.
• Provide technical leadership and solve clinical trial reporting problems within budget and customary time‑line constraints while assuring high quality standards.

Qualifications

Salary

The salary range for this position is expected to be between $205,000 and $230,000 per year. Individual pay may vary based on multiple factors including but not limited to relevant job‑related skills, experience, education or training, market factors, and work location.

Benefits

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.

Equal Opportunity

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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