Novo Nordisk

Lexington, Massachusetts, USA
63,000 Total Employees
Year Founded: 1923
Jobs at Novo Nordisk

Recently posted jobs

19 Hours Ago
Hybrid
Lexington, MA, USA
Artificial Intelligence • Big Data • Machine Learning • Software • Analytics • Biotech • Pharmaceutical
The Manager, Clinical Pharmacology is responsible for developing clinical pharmacology strategies for phases 1-4 of clinical development programs, overseeing dosage and administration strategies, ensuring scientific quality in trials, and facilitating knowledge-sharing as an expert in clinical pharmacology.
Yesterday
Hybrid
Lexington, MA, USA
Artificial Intelligence • Big Data • Machine Learning • Software • Analytics • Biotech • Pharmaceutical
The Senior IT Engineer I - Labs will maintain laboratory IT infrastructure, develop strategies for stakeholder engagement, implement solutions for data capture and storage, and enhance system performance. This role requires extensive collaboration with research teams and internal IT departments.
3 Days Ago
Hybrid
Lexington, MA, USA
Artificial Intelligence • Big Data • Machine Learning • Software • Analytics • Biotech • Pharmaceutical
The Director - Global Regulatory Lead will lead a global regulatory team in developing and executing regulatory strategies for drug development, ensuring high-quality regulatory deliverables and effective communication with stakeholders. This role involves managing health authority interactions, overseeing global filing activities, and maintaining knowledge of regulatory landscapes while fostering team development and accountability.
4 Days Ago
Hybrid
Lexington, MA, USA
Artificial Intelligence • Big Data • Machine Learning • Software • Analytics • Biotech • Pharmaceutical
The Director of Biostatistics leads statistical design, methodology, and analysis for clinical studies, oversees regulatory interactions and filing, and ensures quality deliverables while collaborating with cross-functional teams. They translate statistical concepts into strategic inputs and mentor junior staff.
4 Days Ago
Hybrid
Lexington, MA, USA
Artificial Intelligence • Big Data • Machine Learning • Software • Analytics • Biotech • Pharmaceutical
The Principal Medical Writer will manage the preparation of written deliverables for clinical development and regulatory requirements. Responsibilities include collaborating with cross-functional teams, providing strategic input, authoring and reviewing key regulatory documents, and mentoring other writers. The role demands independent work, strong communication skills, and a comprehensive understanding of clinical research processes.
6 Days Ago
Hybrid
Lexington, MA, USA
Artificial Intelligence • Big Data • Machine Learning • Software • Analytics • Biotech • Pharmaceutical
The Principal Toxicologist will oversee and design toxicology studies, review study protocols, prepare regulatory submissions, and manage toxicology programs in the drug development pipeline.
7 Days Ago
Hybrid
Lexington, MA, USA
Artificial Intelligence • Big Data • Machine Learning • Software • Analytics • Biotech • Pharmaceutical
The Senior Medical Writer is responsible for authoring and editing clinical documents for regulatory submissions, collaborating with cross-functional teams, and ensuring high-quality writing that meets clinical trial requirements. They lead discussions on medical writing issues, review proposed documents, and contribute to process improvements while maintaining knowledge of industry standards and regulations.
9 Days Ago
Hybrid
Lexington, MA, USA
Artificial Intelligence • Big Data • Machine Learning • Software • Analytics • Biotech • Pharmaceutical
The Project Director - Data Lead oversees complex clinical data science projects, defines data strategies, leads project teams, manages internal and external relationships, and ensures the timely execution of data science activities critical to drug development. They drive the use of Target Data Profiles and innovative analytics methods to enhance project outcomes.
10 Days Ago
Hybrid
Lexington, MA, USA
Artificial Intelligence • Big Data • Machine Learning • Software • Analytics • Biotech • Pharmaceutical
The Associate Director of Medical Writing leads the preparation of clinical documentations for regulatory submissions, provides strategic input for development plans, and collaborates with cross-functional teams. Responsibilities include authoring and reviewing documents such as clinical study protocols and submission documents, mentoring less-experienced writers, and ensuring compliance with regulatory standards.
Artificial Intelligence • Big Data • Machine Learning • Software • Analytics • Biotech • Pharmaceutical
The Senior Portfolio Director will drive portfolio strategy, manage cross-functional study teams, oversee clinical trial operations, and ensure compliance with quality standards and budgets. Responsibilities include risk management, performance monitoring, and collaboration with internal and external stakeholders for recruitment and enrollment targets.
22 Days Ago
Hybrid
Lexington, MA, USA
Artificial Intelligence • Big Data • Machine Learning • Software • Analytics • Biotech • Pharmaceutical
The HPC Engineer III will support life-changing medical device research by collaborating with data scientists and researchers to optimize computational workflows, manage HPC environments, provide user training, and propose improvements. This role requires hands-on work with new technologies and maintaining high system performance.