Top Operations Jobs

The Senior Manager - Procurement Digital Enablement is responsible for implementing and driving adoption of digital procurement solutions and technologies to increase productivity and effectiveness.

Responsible for delivering quality clinical research, ensuring patient safety and data reliability in clinical trials. Manages relationships with external and internal stakeholders and drives recruitment and retention strategies for clinical trial sites. Implements risk mitigation plans and ensures compliance with regulatory requirements and guidelines.

Seeking a collaborative and science-driven global regulatory expert to lead a global regulatory team, develop and execute regulatory strategies for high-impact projects, and work with decision-makers across multiple functional areas.

The Therapeutic Area Operations Lead - Cardiovascular is responsible for supporting strategic alignment and consistent therapy area vision between marketing, medical, and market access. This role oversees therapeutic area-specific business operations processes to ensure effective planning and execution to drive business success. Key responsibilities include developing strategies, managing business operations, risk identification and mitigation, resource optimization, and performance tracking.

Lead the strategic execution and continuous improvement of customer experience campaigns through effective leadership, collaboration, and technological integration. Ensure MarTech architecture aligns with business objectives and customer experience priorities. Manage a team of Analysts and drive innovation in campaign execution. Collaborate with cross-functional teams to enhance operational effectiveness and foster a unified customer experience.

The Regulatory Affairs Therapeutic Area Postdoctoral Fellowship at Novo Nordisk is a one-year program based in Plainsboro, New Jersey. The fellow will gain experience in Regulatory Affairs, specifically in the Therapeutic Area with a track for experience in Advertising and Promotion. Responsibilities include assisting in preparation of regulatory documents, working with global stakeholders on FDA submissions, and maintaining up-to-date knowledge of regulations and guidelines.

Contribute to the delivery of Active Pharmaceutical Ingredients (API) by coordinating batch release activities and ensuring timely and efficient release of products. Maintain documentation, verify potency calculations, and facilitate communication among stakeholders. Support problem-solving initiatives and continuous improvement in the release process to meet quality and cost targets.