Vertex Pharmaceuticals Inc. has established a state of the art GMP manufacturing facility in Boston less than a mile from the Corporate Headquarters in the Seaport District. This GMP facility is a keystone to delivering our strategy of bringing transformative medicines to patients in need, from clinical development to commercialization. The Senior Specialist will be respo

The Trade and Distribution Data Analytics Manager will be responsible for supporting insights activities. The insights are used to track business performance and provide key data to inform business decisions. The Manager will typically partner with their manager on key projects and will be responsible for running market research or data analysis. This is a hybrid/on site

Define, plan and execute the full scope of assigned projects. Ability and willingness to perform project tasks at all levels to meet the project needs, from basic to complex, both independently and collaboratively Identify, analyze, prioritize, communicate and mitigate project risks Manage multiple projects simultaneously to successful outcomes Forecast, track and manage

The Principal Biostatistician will perform advanced scientific statistical analyses in support of the company's Global Medicines Development and Affairs area with some guidance and mentoring on new and complex issues. The incumbent will completed work in a resourceful, self sufficient manner and create alternative approaches to achieve desired results. The incumbent shoul

Vertex has established a new research site in Boston Seaport where research, development, and clinical manufacturing for cell and genetic therapies will be primarily based. Cell and genetic therapies represent two rapidly emerging therapeutic modalities with the potential to treat and even cure several of the diseases Vertex is focused on, including sickle cell disease, D

Provides leadership and oversight of DASH/Disease area Safety Team(s) (DST) conduct, for all products across the Vertex Portfolio, including pre FIH activities, key benefit risk assessment, and providing strategy for DSTs to meet goals and objectives. Coordinates and oversees the consistent and timely review of safety data for identification of new safety signals, in acco

The GMP Quality Operations Director serves as a Quality leader in the areas of process validation, and equipment validation in oral solid dosage form. The Director is also responsible for managing multiple department activities with a high degree of independence while providing oversight of the development, implementation, and maintenance of relevant quality initiatives i

The Training Associate Director is responsible for supporting the oversight of all Training related activities within the Global Regulatory Affairs organization. This role will work to create, curate, and deliver top notch learning experiences including both technical and professional development for the team. The Training Associate Director will report directly to the Se

The Director, Modeling & Simulations (M&S) Pharmacometrics will be responsible forindependently determining, planning, and executing M&S analyses for an entire drug development program in close collaboration with cross functional colleagues within the R&D organization. In this role, it is expected that the incumbent will represent M&S with cross functional drug developmen

Build and manage a manufacturing engineering team for DSDP cells and combination products Act as primary technical and engineering manufacturing lead design reviews, documentation with focus on designing for manufacturability. Implement, propose and drive the implementation of Drug Product Device and manufacturing engineering controls by integrating Vertex QMS, production

Provides comprehensive expertise and guidance in designated therapeutic area(s) and Vertex medicines Leads a team of physicians and scientists to create and execute appropriate medical affairs plans and tactics supporting designated therapeutic area(s) and Vertex medicines Develops and maintains professional relationships with local Health Care Professionals, and with loc

Independently performs content, editing, and formatting QC of moderately complex regulatory and clinical study documents, which may include complex CSRs, complex protocols, Investigator Brochures, and single study Module 2 summaries Ensures QC reviewed documents are compliant with MWS Style guide and templates Troubleshoots MWS processes, tools, and technologies and may s

Within assigned area, designs, develops and executes the technical/statistical infrastructure for the conduct and evaluation of clinical trials, observational studies, or real world data (RWD) investigations, including related areas/activities. Participates in regular Study Execution Team (SET) team meetings as the functional representative. Works under supervision to aut

The Corporate Finance Associate Director is a key member of Vertex's Finance organization, supporting the annual budgeting and monthly forecast processes including the analysis, preparation, and communication of financial results to the CFO leadership team. The role will collaborate closely across Finance and other teams to identify and deliver actionable insights that dr

Lead all activities related to the engagement and account management of assigned accounts i.e., national/regional wholesalers and distributors and/or national specialty and retail community pharmacies. Negotiate, implement and manage Specialty Pharmacy Master Service Agreements (MSAs), Enhanced Service Agreements (ESA), Retail Stocking Agreements (RSA), and Distribution S