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.

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 Director, Bioanalytical / Biomarkers will lead the strategy, development, and execution of bioanalytical and biomarker assays to support clinical development programs.

This role is responsible for advancing translational insights, enabling decision-making through high-quality data, and ensuring regulatory-compliant bioanalytical operations across studies.

Key Responsibilities

Strategy Leadership Define and execute bioanalytical and biomarker strategies across preclinical and clinical programs Align biomarker plans with clinical, regulatory, and development objectives Serve as a subject matter expert in bioanalysis and translational biomarkers Assay Development Oversight Oversee development, validation, and implementation of bioanalytical assays (e.g., PK, ADA, cell-based, molecular assays) Guide biomarker assay selection and fit-for-purpose validation strategies Ensure assay performance meets regulatory and scientific standards Vendor Study Management Select and manage CROs and external labs for bioanalytical and biomarker activities Oversee timelines, budgets, and deliverables across studies Ensure high-quality data generation and timely reporting Clinical Study Support Partner with Clinical Operations and Clinical Development to integrate biomarker endpoints into study design Review and interpret biomarker and PK/PD data to inform program decisions Contribute to clinical study protocols, SAPs, and reports Regulatory Compliance Ensure compliance with GLP/GCP and regulatory guidance (FDA, EMA) Contribute to regulatory submissions (INDs, BLAs, briefing packages) Represent bioanalytical/biomarker strategy in regulatory interactions as needed Cross-functional Collaboration Work closely with Translational Sciences, Clinical Pharmacology, Regulatory, and CMC teams Communicate complex data and insights to internal stakeholders and leadership

Qualifications

PhD in Biology, Pharmacology, Immunology, Bioanalytical Sciences, or related field (or MS with significant experience) 10+ years of experience in bioanalysis and/or biomarker development in biotech/pharma Deep expertise in bioanalytical assays (e.g., LC-MS/MS, ELISA, flow cytometry, qPCR, NGS, cell-based assays) Strong understanding of PK/PD, immunogenicity, and translational science principles Experience supporting clinical-stage programs and regulatory filings Proven track record managing CROs and external partnerships Strong leadership, communication, and project management skills

Preferred Qualifications

Experience in [oncology, cell/gene therapy, immunology — tailor as needed] Familiarity with companion diagnostics or advanced biomarker platforms Prior team leadership or people management experience The salary range for the Director, Bioanalytical / Biomarkers is expected to be