Top Operations Jobs
The Medical Affairs Postdoctoral Fellowship at Novo Nordisk is a one-year program based in Plainsboro, New Jersey. The fellow will gain practical experience in the pharmaceutical industry, working on various projects and developing skills to contribute to customer needs and company goals. Responsibilities include leading projects, developing scientific materials, understanding industry regulations, strategic planning, and providing medical information to healthcare professionals.
Manage and implement compensation programs to meet organizational objectives with regards to internal equity and external market competitiveness. Provide guidance on total rewards policy, analyze market data, and develop salary budgets. Collaborate with HR partners and global COE to create and implement rewards initiatives. Report to Vice President, Total Rewards - North America and interact with various teams and external partners.
The Vice President of Medical and Science is responsible for providing leadership and direction to the Medical and Science Area East Coast Hub team, ensuring strategic partnerships in clinical drug development activities, and setting medical strategic direction for various projects. This executive role involves overseeing medical and scientific issues related to drug and device development, interacting with authorities, and ensuring data integrity in clinical trials.
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Seeking a highly experienced procurement leader with marketing expertise to lead the TA and Commercial Category Procurement team within Novo Nordisk Inc. Responsibilities include developing sourcing strategies, collaborating with stakeholders, and driving business priorities for each TA partnership.
The Senior Director - Clinical Pharmacology at Novo Nordisk is responsible for developing clinical pharmacology strategies for phase 1-4 clinical development programs, dosage and administration strategies, and overseeing scientific and pharmacology aspects of trials. This role involves cross-functional collaboration and may require travel. The position reports to the VP of Medical & Science for the U.S. East Coast Hub and involves interaction with various teams within the organization.
Lead process development for enzymatic ligation of oligonucleotides and biocatalytic processes pertaining to RNA synthesis. Contribute to sustainable manufacturing of oligonucleotides and collaborate with internal and external teams for research projects.
Develops and executes pricing and contracting strategy for Novo Nordisk product category, collaborating with internal and external stakeholders to ensure market access objectives are met. Manages relationships with various teams and stakeholders, participates in optimization of contracting strategy, and monitors pharmaceutical pricing environment in the US.
Manage and oversee all assigned projects/products/processes in Regulatory Affairs, ensuring compliance with internal SOPs and regulations. Develop positive relationships with internal and external stakeholders, including FDA personnel. Responsibilities include compiling and submitting responses to FDA communications, maintaining product/project databases, liaising between departments, staying updated on regulations, managing development projects, and supervising labeling approval for marketed products.
The Scientific Director at Novo Nordisk is a subject matter expert supporting strategic projects aligned to Therapy Area priorities. Responsibilities include trend identification, project management, customer knowledge enhancement, clinical trial support, stakeholder evaluation, and cross-functional collaboration. The role involves direct customer engagement activities and coordination with key functions across the organization.
Develops and executes pricing and contracting strategy for a key product category at Novo Nordisk. Collaborates with internal and external stakeholders to ensure market access business objectives are met. Supports new product launches, develops pricing scenarios for pipeline products, and assesses investments in payer contracts.
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