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As a Medical Advisor, you will implement the medical affairs strategy, drive real world evidence generation, engage with KOLs, and support regulatory activities for new product launches related to diabetes management.
As a Senior Market Access Manager, you will develop and execute market access strategies, lead brand payer value story development, negotiate pricing for public and private listings, and manage reimbursement submissions. You will also collaborate with internal and external stakeholders to enhance access for patients with chronic diseases.
This job is for candidates aspiring to become Associate Managers across various teams in Novo Nordisk, including Production and IT. Applicants will be matched with suitable positions based on their skills and interests, emphasizing leadership qualities and team management. Fluency in Danish or English is required, and experience in regulated industries is preferred.
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As a Student Assistant in the Engineering and Business Support Talent Pipeline at Novo Nordisk, you will assist with projects to improve manufacturing setup, support innovative technology use, and work across departments in areas such as data engineering, software engineering, and automation while gaining practical experience.
Join our Talent Pipeline for Student Assistant positions in Pharma and Biotechnology. Work alongside professionals in R&D, Clinical Science, and Regulatory Affairs. Ideal candidates are pursuing a Bachelor's or Master's in Life Sciences, eager to learn and have lab experience. Flexible hours allow for academic commitments.
The Procurement Professional at Novo Nordisk will manage vendor registrations, contract agreements, and purchase orders. Responsibilities include processing vendor applications, managing invoices, supporting cash flow, and acting as a Subject Matter Expert during audits while ensuring compliance and sustainability in procurement practices.
The Administration Staff at Koriyama Factory will enhance the work environment for employees by handling administrative tasks, overseeing health and safety initiatives, managing vendor relationships, and promoting organizational goals. This role involves effective communication both internally and with external stakeholders, and supporting health management programs.
As a Regional Medical Advisor, you'll engage with HCPs, lead educational initiatives, and support brand strategy development. Responsibilities include conducting field visits to gather insights, leading training for stakeholders, managing scientific events, ensuring compliance, and reporting safety issues according to SOPs.
As a Safety Surveillance Adviser, you will oversee the safety profile of products during development and after approval, communicate drug safety issues, maintain product labelling, prepare safety reports, and respond to health authorities. You will actively participate in safety committees and provide project safety communication, ensuring compliance with regulatory standards.
As a Clinical Medical Manager Lead, you will oversee the CMM team activities, ensuring they possess the skills necessary for clinical trial execution. Responsibilities include engaging with experts in relevant therapy areas, delivering medical guidance, supporting clinical trials, and facilitating communication with local stakeholders.
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