Vor Bio

HQ
Cambridge
175 Total Employees

Jobs at Vor Bio

Let Your Resume Do The Work
Upload your resume to be matched with jobs you're a great fit for.

Recently posted jobs

13 Days AgoSaved
In-Office
Boston, MA, USA
Biotech
Lead enterprise data and AI strategy and build scalable data infrastructure for a biotech company. Deliver prioritized AI use cases, enable productivity tools, ensure regulated data and AI controls, and partner cross-functionally to create reporting, governance, and analytics that support clinical, regulatory, medical affairs, commercial, and executive decisions.
13 Days AgoSaved
In-Office
Boston, MA, USA
Biotech
The Senior Accountant will manage day-to-day finance operations, prepare journal entries, oversee financial reporting, and ensure compliance with internal controls.
16 Days AgoSaved
In-Office
Boston, MA, USA
Biotech
Lead end-to-end clinical trial management for complex autoimmune studies, ensuring ICH/GCP compliance, CRO/vendor oversight, site and PI selection, budget and timeline control, risk mitigation, quality/audit readiness, and mentoring of clinical team members to deliver trials on time and within budget.
16 Days AgoSaved
In-Office
Boston, MA, USA
Biotech
Lead scientific support for global clinical trials from design through database lock. Prepare and review study documents, support medical monitoring and safety review, define risk and monitoring plans, ensure eCRF/protocol alignment, drive data cleaning and validation, collaborate cross-functionally (Medical, PV, Clinical Ops), and support trainings and regulatory/IRB interactions to ensure data quality and scientific integrity.
17 Days AgoSaved
In-Office
Boston, MA, USA
Biotech
Lead end-to-end clinical operations for autoimmune programs, managing study budgets, timelines, CROs/vendors, regulatory compliance (ICH/GCP), TMF/eTMF oversight, inspection readiness, cross-functional coordination, and mentorship of clinical trial staff to ensure successful execution of Phase II/III trials.
19 Days AgoSaved
In-Office
Boston, MA, USA
Biotech
Lead global Regulatory CMC strategy for biologics and combination biologic/device programs. Drive CMC submissions (INDs/CTAs, amendments, registrations), negotiate with regulators, manage timelines, vendors, and inspection/change control activities, and provide cross-functional regulatory guidance across process, analytical, formulation, and lifecycle management to support clinical development and global registration.