Senior Data ManagerVor Biopharma Inc. • Boston, Massachusetts, United States
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Senior Data Manager
Vor Biopharma Inc.
- Boston, Massachusetts, United States
- Boston, Massachusetts, United States
À propos
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 Senior Data Manager is responsible for all 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 bodies. In addition, the Senior Data Manager has an active role in continuous improvement and acts as a leader in the department as demonstrated by successful mentoring and consistent study delivery over time.
Responsibilities:
* 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 cycle i.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
Compétences linguistiques
- English
Avis aux utilisateurs
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