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Managing and overseeing document control and archives operations, leading global teams, projects, and initiatives, providing coaching and guidance to employees, supporting manager with data and analysis, and ensuring optimal design of the team and operations.

The Senior Manager / Manager Supply Operations will be responsible for facilitating batch disposition and order management activities to ensure timely product supply. They will use a data-driven approach to drive process improvements and communicate global supply operations performance to senior management. This role requires a Bachelor's degree in Business, Engineering, Supply Chain Management, or Science and 6+ years of relevant pharmaceutical/biotechnology experience.

The Manager, Statistical Programming will lead and support all programming activities within therapeutic areas, ensuring timely project implementation and high-quality results. Responsibilities include coordinating programming documentation, acting as a technical resource, supporting regulatory submissions, and mentoring junior programmers. Proficiency in SAS programming, clinical data environment, and pharmaceutical clinical development are required. Must have an MS (or BS) in Statistics, Computer Science, Mathematics, or related field with 8+ (9+) years of programming experience in the biotechnology, pharmaceutical, or health-related industry.

The Senior Manager Market Access will oversee HTA submissions, price negotiation, and market access strategies in Benelux & Nordic markets within a global pharmaceutical company. Responsibilities include collaborating on dossiers, developing pricing strategies, and supporting new product launches. The role requires 8+ years of relevant industry experience and a scientific degree.

The Principal IT Applications Analyst for Digital Products is responsible for assessing and planning innovation initiatives involving new and emerging technology. This role drives initiatives from conceptualization, evaluates new technologies, coordinates teams, and serves as the main technologist point of contact. Responsibilities include working with IT management and clients to identify business requirements, collaborating with various teams and vendors, resolving challenges, and staying informed on emerging technologies.

The Senior Manager, Central Monitoring is responsible for centralized monitoring activities for global and/or complex trials, analytical data review, interpretation of Key Risk Indicator (KRI) and Key Performance Indicator (KPI) data, presenting findings, and driving process improvement in central monitoring capabilities.

The QA Supplier Specialist at Regeneron is responsible for ensuring the quality of raw materials used in drug production, managing supplier relationships, and supporting various quality assurance initiatives. They analyze testing results, implement process improvements, and maintain project timelines. Requires a BS/BA in business or life sciences and 2+ years of experience.