The Analytical and Purification Principal Research Associate will lead the small molecule chiral purification platform within the Medicinal Chemistry group. The individual will propose and develop improvements in the purification workflow along with implementing new software and hardware technologies for high throughput separations. In addition, the successful applicant w

This position is responsible for establishing and managing a global occupational and environmental toxicology program. The individual will be required to provide stewardship and support for Vertex's project portfolio. The individual will be part of the global environmental health and safety (EHS) team responsible for setting standards, developing culture and programs esta

Vertex Cell & Genetic Therapies (VCGT) is seeking a highly skilled and motivated Translational Engineering Senior Scientific Associate to join the Biomechanics Research team in Providence, RI. The team's mission is to design and develop biomechanical strategies to enable cell based delivery technologies for the treatment of type 1 diabetes. We are looking for a candidate

Establishes meaningful and professional relationships within key accounts across multiple layers of the hospital system (key hospital medical and administrative staff, pharmacies, formulary decision makers and KTLs) Develops and maintains expertise on the product's clinical attributes and patient unmet need and educates healthcare professionals on product use in appropria

P lay a critical role in setting up in house chargeback function , working cross functionally with 3 PL, Trade & Distribution, Accounting, and DTE, etc. to develop policies, efficient processes, system requirements, and department al SOPs . Partner with Government Pricing & Programs , Contract Operations , Payer Accounts and Legal, etc. to p rovide key insights during con

Lead and ensure successful development and implementation of the commercialization (midterm) and portfolio (long term) strategies including brand development, competitive strategy, go to market/launch, and lifecycle decisions for future launches. Execute in close partnership with the Regions, Market Access, Regulatory and Commercial Manufacturing. Deliver foundational ins

The Senior Director, Quality GLP, Biomarkers and Research has overall accountability for strategic leadership and oversight of the end to end quality assurance strategy for proactive, risk informed, and sustainable quality oversight and compliance with regulatory expectations across Vertex processes for clinical evidence generation and product vigilance Key Duties and Res

Establishes meaningful and professional relationships within key accounts across multiple layers of the hospital system (key hospital medical and administrative staff, pharmacies, formulary decision makers and KTLs) Develops and maintains expertise on the product's clinical attributes and patient unmet need and educates healthcare professionals on product use in appropria

Establishes meaningful and professional relationships within key accounts across multiple layers of the hospital system (key hospital medical and administrative staff, pharmacies, formulary decision makers and KTLs) Develops and maintains expertise on the product's clinical attributes and patient unmet need and educates healthcare professionals on product use in appropria

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

Stay current with 340B program regulation s and guidelines , trends, and public policy ruling s at the Federal, State, and local level in collaboration wit h Government Pricing, Policy, and Legal teams . S upport analysis on potential impact assessments and 340B program general education of internal stakeholders. Responsible for managing 340B Customer Master eligibility s

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

Identifying, assessing, and acquiring third party data sources (e.g., IQVIA, Symphony, Definitive, Clarivate, etc.) to provide the most appropriate data required to support and inform commercial business decisions. Act as the subject matter expert on all of these data sources. Manage and develop relationships with third party data vendors. Responsible for creation and enh