Senior Data Manager

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.

The Senior Data  Manageris responsible forall data management activities from study start-up through database lock and archiving and independently supporting the needs of the clinical study and programs of studies.

The Senior Data  Manager will ensure completeness,accuracy and consistency and meet the standards of quality analysis and reporting to regulatory  addition, theSenior

Data Manager has an active role in continuous improvement and acts as a leader in the department asdemonstratedby successful mentoring and consistent study delivery over time.

• Serves as data lead for one or more clinical trials, assuming responsibility for all data management activities, including access levels and permissions.
• Proactively drive quality and efficiency to meet timelines and milestones for data management in close collaboration with cross functional study team(s)
• Conduct oversight of data management activities internally and performed by the CROs and other 3rd party vendors (IRT, Safety, Lab, etc.) to meet Vor obligations and business objectives throughout study (ies) life cyclei.e.from protocol synopsis through database release and submission.
• Serve as a first point of contact for DM partners to ensure established milestones and deliverables are met with the highest degree of quality
• Ensure the internal and external partners align and conform to data management expectations for the assigned compound and/or indication.
• Review and provide input for all DM documentation - CRF design and completion Guidelines, Data Management Plan, Data Transfer Specifications, etc.
• Oversee edit check specifications to support data collection and analysis required per protocol.
• Ensure the clinical database adheres to Clinical Data Acquisition Standards Harmonization guidelines allowing for optimal SDTM dataset programming. Suggest design for standard and non-standard data collection, identify any gaps in data collection, and challenge collection of unnecessary data.
• Participate in the creation of the clinical development plan, describing the clinical development strategy and possible innovative trial designs.
• Set quality expectations and timelines for data management deliverables and regularly follow up on data management milestones. Ensure inspection readiness at all times.
• Set expectations and communicate and a transparent, clear way and motivate team members to work towards achieving the clinical goals.
• Follow department and company standard operating procedures (SOPs), forms, templates and policies. Provide feedback and update these guidelines as needed.
• Develop,…