Overview 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. 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 Data Manager duties from study start-up through database lock, archiving, and independent support of the clinical study and programs of studies. Ensure completeness, accuracy, and consistency of data; meet quality analysis and reporting standards for regulatory bodies. Act as a leader in the department with mentoring and consistent study delivery; contribute to continuous improvement. Ensure CRO and internal/external partners align with data management expectations for assigned compound and/or indication. Participate in creation of the clinical development plan and describe the clinical development strategy and innovative trial designs. Set quality expectations and timelines for data management deliverables; maintain inspection readiness. Communicate clearly to motivate team members toward clinical goals; adhere to SOPs, forms, templates, and policies; provide feedback to update guidelines as needed. Develop, review, and maintain all study Data Management documentation. Coordinate with Database Developers for effective database build and timely go-live. Ensure the clinical database adheres to CDASH/SDTM standards; identify gaps and optimize data collection. Define eCRF and edit check specifications to support data collection and analysis per protocol. Oversee QC and UAT of the clinical database prior to production release, including supervision of staff performing these tasks. Ensure data are reviewed per the Data Management Plan and cleaned timely. Provide input on study timelines, risks, and mitigation strategies; contribute to process efficiency improvements. Lead or participate in intradepartmental or interdepartmental process and quality improvement initiatives. Requirements Bachelor’s Degree in programming, health-related sciences, or relevant field; 5+ years of Data Management experience. Excellent verbal and written communication skills; professional attitude and strong interpersonal skills. Ability to work with a multi-disciplinary team; flexible, with ability to adapt to new learning. Ability to prioritize workload; understanding of clinical research and Data Management role in the study process. Strong technical aptitude and ability to adapt to multiple data management platforms; strong knowledge of electronic data capture (EDC) systems. Good computer skills (Microsoft Word, Excel, and PowerPoint) and ability to understand and adapt to various IT systems. Benefits & EEO Vor supports its 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 well-being so you can thrive at work and beyond. As an equal opportunity employer, Vor Bio does not discriminate on the basis of race, age, color, religion, sex, sexual orientation, gender identity, national origin, veteran or disability status. All applicants will be considered for employment agnostic to protected status. Please visit our website at for more information. #J-18808-Ljbffr Vor Bio
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