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The Senior Manager of Advertising Promotion is responsible for regulatory reviews related to advertising and promotional communications for healthcare audiences. This role ensures compliance with regulations, provides regulatory guidance to commercial teams, facilitates cross-functional discussions, monitors advertising regulations, and conducts training sessions.
The Project Management and Strategic Operations Manager will lead projects in advanced analytics and AI solutions for business questions within the life sciences and healthcare industries. Responsibilities include developing project plans, managing deliverables, communicating with stakeholders, and driving data-driven innovation. Qualifications include an MBA with relevant experience in statistics, mathematics, computer science, or related life sciences disciplines.
As a Principal Scientist in Analytical Development at Vertex, you will design and oversee drug substance process development, focusing on quality control strategies, regulatory submissions, and analytical methods. You will collaborate with various teams, act as a subject matter expert, and manage a small group while developing innovative solutions to challenges in drug substance development.
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 Global Head of Market Access for Povetacicept will lead the pricing and access strategy for a new treatment for IgAN, ensuring launch readiness and developing evidence plans. This role demands collaboration across teams and responsibility for managing direct reports and advancing global payer strategy.
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.
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