Provides comprehensive expertise and guidance in the Therapeutic Area and Vertex drugs Develops and maintains professional relationships with local Health Care Professionals, and with local Professional Societies and Patient Advocacy groups. Establishes relationships with Thought Leaders to expand research opportunities for Vertex and develops, at local level, advisory, c

The Director, Regulatory CMC (Chemistry Manufacturing Controls) is responsible for the development and implementation of post approval global regulatory CMC strategies for a marketed cell and gene therapy product. This role provides regulatory guidance to various cross functional teams to ensure all applicable global regulatory requirements are considered and appropriatel

Vertex's Data, Technology and Engineering (DTE) team is seeking a Manufacturing and Supply Chain (MSC) Technology Portfolio Manager to join our Project Management and Strategic Operations group. Project Management and Strategic Operations is charged with streamlining and simplifying the work of our data and technology teams and ensuring the successful deployment of new te

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 is seeking a talented Process Engineering Senior Scientific Associate to join our Process Development team. This individual will support late phase cell therapy process development, including performing process optimization activities, and characterization of a cell based product for ongoing and future projects. This role may contribute to the exploration and estab

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

The Executive Director, Pain Global Strategy will have global responsibility to build the Global Medical strategy for Pain assets. Communicate the Global Medical strategy to partner functions for further strategic and tactical guidance. Execute the Global components of the medical strategy plan. Partner with Clinical Development, HEOR, RWE, Regional Medical Affairs and pa

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

Responsibility to build and execute the Global Medical strategy for key CF products. Communicate the Global Medical strategy to partner functions and senior leaders for further strategic and tactical guidance. Execute the Global components of the medical strategy plan. Partner with Clinical Development, HEOR, RWE, Regional Medical Affairs and partner functions to identify

Authors complex clinical regulatory documents (e.g., clinical study protocols, clinical study reports, investigator's brochures, documents to support meetings with regulatory agencies, and sections of marketing authorization applications) in partnership with key stakeholders Serves as the lead Medical Writing Scientist for complex or pivotal clinical studies for multiple

The Director, Manufacturing Technical Services, Quality Assurace is responsible for the quality oversight of Contract Manufacturing Organizations (CMOs) and Contract Test Labs (CTOs) for Cell & Genetic Programs through the lifecycle development process. This includes quality oversight for the selection, qualification and routine monitoring of Contract manufacturers and la

The Associate Director, Regulatory CMC executes multi product global regulatory CMC strategies for cell therapy combination investigational and marketed products. This role leads the preparation and filing of regulatory CMC submissions and manages the interactions with Health Authorities for CMC topics. This role also provides regulatory guidance to various cross function

As a key member of the Corporate/North American accounting department, the General Ledger Senior Accountant II partners with members of the accounting and finance departments as well as teams across other departments throughout the Company. The position provides exposure to key accounting and reporting areas and offers development opportunities that can lead to advanced r

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