Search the 13 jobs at Vertex Pharmaceuticals

The Senior Protein Engineer Scientist will design and execute protein engineering campaigns using yeast surface display and computational design tools to optimize protein drug candidates. This role involves collaboration with cross-functional teams, preparing reports and patents, and advancing therapeutic developments.

The Senior Manager of Quality Operations will oversee quality assurance management processes, including product investigations, risk management, and continuous improvement initiatives. This role involves collaboration with cross-functional teams, support during inspections, and leadership in compliance with medical device regulations.

The EHS & Sustainability Senior Manager oversees various EHS programs at a site, engaging with teams to integrate policies, manage audits, vendor relationships, and health initiatives. The role requires strong communication, problem-solving skills, and leadership in safety and environmental issues while preparing metrics and handling budgets.

The Principal Biostatistician will perform advanced statistical analyses in support of Global Medicines Development, represent Biostatistics in clinical trial teams, develop statistical analysis plans, collaborate with cross-functional teams, and contribute to various publications.

The Territory Account Manager in Charleston, West Virginia will establish and maintain relationships with key institutional decision makers and healthcare professionals to drive sales growth for the US Pain Business Unit. Responsibilities include engaging with key accounts, educating healthcare professionals on product attributes, navigating formulary processes, and developing strategic account plans for business growth. The role requires expertise in IT capabilities and CRM, as well as collaboration with field teams and HQ colleagues for business alignment and compliance.

The Senior Manager, Revenue Accounting will oversee financial information related to product revenues, gross to net accounts, and accounts receivable for the North America Region. Responsibilities include month-end close, developing gross to net models, collaborating on actualization and forecasting, driving process improvements, and overseeing team members.

The Real World Principal Biostatistician will perform advanced scientific statistical analyses in support of the company's post-marketing areas for Global Medicines Development and Affairs, and Commercial and Strategic Management, with some guidance and mentoring on new and complex issues.

The Global Spend Transparency Analyst plays a critical support role in supporting the Global Spend Transparency team by owning reports, analyzing datasets, maintaining dashboards, and ensuring regulatory compliance. Strong analytical and communication skills are essential for this role.

The Principal Statistical Programmer at Vertex is responsible for leading project teams, providing technical expertise in SAS programming, ensuring compliance with regulations, and supporting clinical trial reporting. They collaborate with cross-functional teams to create documentation for data analysis and submission activities.

The Strategic Sourcing Director for Small Molecules will lead sourcing efforts for materials and services, develop category strategies, manage key suppliers, and drive continuous improvement to deliver exceptional value to the company and patients. This high-visibility role involves collaborating with stakeholders, overseeing market analysis, negotiation, and risk management, and optimizing sourcing processes.

Lead the Preclinical Pharmacology team in designing and executing pharmacology studies to support Type 1 diabetes cell therapy programs. Provide strategic oversight, resource management, and mentorship to the team. Ensure the quality and integrity of all preclinical research activities.

The Senior Administrative Assistant provides experienced and end to end administrative support to the CF Commercial Strategy VP and the international GIACO Senior Director and their respective teams. Responsibilities include managing calendars, handling internal technologies, exchanging information, booking travel, preparing meeting materials, assisting with office operations, and maintaining confidentiality. Requires established knowledge of Microsoft Office, time management skills, attention to detail, and discretion in handling sensitive information.

The Senior Specialist, GxP Site Engineering will serve as the primary point of contact for all engineering needs in a Cell and Gene Device Manufacturing Facility. Responsibilities include collaborating with various teams, implementing strategic decisions for capital projects, providing regulatory support, and ensuring engineering KPIs are met. Required skills include knowledge of cGMP, facility design, and regulatory compliance.