Novo Nordisk

Support Engineer

• Leading and/or participating in validation activities of our new aseptic filling line
• Ensuring full compliance with validation, GMP, and quality requirements throughout all technical activities
• Help prepare our department and technical processes for a robust operational setup
• Applying an innovative mindset and LEAN approach to continuously improve processes and equipment performance
• Ensuring a robust foundation for our rep team by assisting in e.g. the development of Maintenance Work Descriptions, Training Outlines, updating or developing new technical SOPs, setup of maintenance structures and content in SAP

Technical Supporter – New Filling Line, Maternity Cover

Clinical Operations

• Lead a team that transforms clinical trial execution into measurable impact for patients worldwide
• Provide strategic oversight and line management of clinical operations staff
• Ensure high performance and professional development of clinical operations staff
• Drive operational excellence across clinical trial execution
• Define and track performance metrics such as site visits, milestone completion, and data quality
• Conduct co-monitoring and quality visits with CRAs to ensure quality oversight and protocol adherence
• Collaborate with cross-functional teams to align on resourcing, study priorities, timelines, and operational execution
• Embed Risk-Based Quality Management principles within the clinical operations team
• Ensure all clinical operations activities comply with ICH-GCP, applicable regulations, and internal SOPs

Manager, Clinical Operations

Production Engineer

• Perform hands-on setup, operation, and program edits for CNC and manual machines producing components for API manufacturing, following controlled procedures and documentation practices.
• Support process stability by performing first-article and in-process inspections, maintaining tooling and fixtures, and escalating process or quality issues to senior engineers.
• Develop practical CAM skills in Fusion 360, learn regulatory and GMP requirements for product-contact parts, and contribute to continuous improvement activities.
• Execute CNC programs and perform machine setups and changeovers per work orders and documented procedures.
• Use Fusion 360 for CAM edits, program creation from approved templates and execute offline program verification where required.
• Optimize machining processes to improve efficiency, accuracy, and repeatability.
• Develop, modify, and optimize CNC tool paths using CAM software.
• Program parts from engineering drawings, 3D models, and physical samples.
• Troubleshoot and refine CNC programs to resolve quality, tooling, or cycle-time issues.
• Reverse engineer components using measurements, drawings, or physical samples to develop accurate CAD models and machining strategies.
• Perform in-process and final quality checks using precision measuring tools (e.g., calipers, micrometers, gauges) ensuring parts meet all dimensional, tolerance, and surface finish requirements and document results in accordance with local quality procedures.
• Write, review, and follow Standard Operating Procedures (SOPs) related to machining, programming, inspection, and maintenance.
• Provide hands-on training and technical guidance to Novo Nordisk personnel on CNC machining, programming, setup, and inspection.
• Perform minor CNC machine maintenance, including routine cleaning, lubrication, alignment checks, and basic troubleshooting.

CNC Production Engineer I

Product Marketing

• Secure existing & future supply of GMP materials to Novo Nordisk production sites through transfer of materials between existing production entities whilst expanding new materials & new suppliers.
• Responsible for implementation of new materials and supply chains for GMP Materials
• Responsible for GMP materials qualification including change control, risk assessment of incorporation of material, material specification plan, evaluation of GMP Material with regards to animal origin, supply chain qualification statement and creation of item number in SAP for incoming materials for production in Novo Nordisk US
• Support setting the specifications for our materials based on the use at Novo Nordisk to ensure compliance & patient safety and handle requests
• Participation in approval of new materials & new suppliers
• Support & contribute to the quality control strategy for new materials
• Evaluating material change notifications from suppliers
• Handle requests and questions regarding specific materials
• Involved in maintenance and life cycle management of GMP Materials including owning change requests, and owning actions
• Perform minor deviation investigations for material issues
• Follow all safety & environmental requirements in the performance of duties
• Other duties as assigned

GMP Material Professional

Research Analyst

• Oversee and manage assigned clinical trial sites, conducting on-site and remote monitoring visits to ensure compliance with protocols, ICH-GCP guidelines, and regulatory requirements
• Drive the implementation of Risk-Based Quality Management (RBQM) principles to proactively identify, assess, and mitigate risks throughout study conduct
• Build and maintain strong relationships with investigators, site staff, and cross-functional teams to support efficient clinical trial execution
• Monitor site performance, recruitment progress, retention, and data collection to ensure study timelines and quality objectives are met
• Ensure patient safety and data integrity by resolving discrepancies, managing adverse events, and maintaining inspection readiness
• Provide site training and continuous support on study protocols, operational procedures, systems, and compliance requirements
• Act as an ambassador for Novo Nordisk values at the site level, ensuring high-quality trial execution

Clinical Research Associate

Medical Director

• Lead the medical strategy that brings breakthrough cardiovascular treatments from clinical trials to patients worldwide
• Engage in Launch Activity Plans, Therapeutic Area Development Strategy, and Go-To-Market Strategy to make future cardiovascular products a success
• Collaborate cross-functionally with Commercial, Market Access, Marketing, Clinical Development and other functional areas
• Engage with Key Opinion Leaders (KOLs) in various settings, focusing on medical and scientific information to optimize product development and patient treatment
• Provide medical input to clinical trial development, including investigator selection, and drive scientific dialogue based on trial results
• Develop publications based on clinical trial results
• Advise and drive the development of internal and external medical guidance and educational materials
• Present data at internal forums and external conferences, supporting the Medical Director in strategic and leadership tasks

Global Associate Medical Director – Cardiovascular Disease

Director

• accountable for setting the strategic medical stakeholder engagement plan
• execution of these plans for medical affairs
• leading without authority to drive and deliver against key business goals
• establishing the NN medical presence with assigned stakeholders
• supporting external medical/market development
• strategic stakeholder engagement plans for groups associations, congresses, partners, and other stakeholder groups relevant to medical affairs
• focused on increasing disease awareness, improving screening and diagnosis, and/or informing medical management

Director Stakeholder Engagement

• Oversee and manage assigned clinical trial sites, conducting on-site and remote monitoring visits to ensure compliance with protocols, ICH-GCP guidelines, and regulatory requirements.
• Drive the implementation of Risk-Based Quality Management (RBQM) principles to proactively identify, assess, and mitigate risks throughout study conduct.
• Build and maintain strong relationships with investigators, site staff, and cross-functional teams to support efficient clinical trial execution.
• Monitor site performance, recruitment progress, retention, and data collection to ensure study timelines and quality objectives are met.
• Ensure patient safety and data integrity by resolving discrepancies, managing adverse events, and maintaining inspection readiness.
• Provide site training and continuous support on study protocols, operational procedures, systems, and compliance requirements.
• Act as an ambassador for Novo Nordisk values at the site level, ensuring high-quality trial execution.

Project Manager

• Leading medium‑complexity product development and LCM projects with accountability for quality, cost and timelines
• Defining project scope, success criteria, plans and critical paths in alignment with portfolio priorities
• Managing internal and external stakeholders, including external development partners where relevant
• Driving effective cross‑functional collaboration, communication and decision‑making
• Contributing to scenario planning and portfolio decisions across the CVP+ area

Operations

• Partnering closely with Market Access, Public Affairs and Patient Support Solutions (MAPA & PSS) leadership
• Representing the core vision and values in the planning and facilitation of department meetings, communications and annual training plan
• Collaborating with broader teams to execute activities in support of the MAPA organization
• Responsible for Communication/Messaging across all of MAPA and other key internal stakeholders
• Developing MAPA’s annual training plan and ensuring all communications are executed compliantly

Senior Operations Enablement Manager

• Provide strategic oversight and management of clinical trial sites within CDC and Ad Hoc affiliate
• Drive study quality and performance through risk-based monitoring and proactive risk management
• Collaborate effectively with site staff and cross-functional teams to ensure successful execution of the trial
• Conduct on-site and remote monitoring visits in accordance with the Monitoring Plan, Protocol, ICH-GCP, internal SOPs, and applicable regulatory requirements
• Drive the implementation of RBQM principles to ensure high-quality execution of clinical trial activities
• Actively engage with site staff and collaborate with cross-functional teams to support strong site relationships and ensure efficient clinical trial execution

• Responsible for end-to-end site management and monitoring activities in Phase II–III clinical trials
• Ensuring compliance with ICH-GCP, protocol requirements, and Novo Nordisk procedures
• Serving as the primary liaison between Novo Nordisk, clinical sites, and study teams
• Conducting on-site and remote monitoring visits to ensure protocol compliance
• Managing sites across the trial lifecycle (selection, initiation, conduct and close-out)
• Driving inspection readiness and high-quality documentation
• Building strong, trusted partnerships with new and existing sites
• Supporting patient recruitment and retention initiatives at site level
• Using digital tools and systems effectively to plan, execute and document monitoring activities
• Maintaining accurate trial documentation, including the Investigator Trial Master File, and ensuring inspection readiness throughout all trial stages

Administrative Assistant

• Performs a variety of highly diverse and complex administrative tasks and activities
• Directly supports two or more individuals
• Coordinates multiple processes, procedures, or programs
• Develops reports and presentations
• Hands calendar management on behalf of the individuals supported
• Participates on, and provides administrative support to, project teams
• Handles routine office duties including data entry, meeting/travel arrangements, and budget processing

Administrative Specialist

• Oversee and manage assigned clinical trial sites, conducting on-site and remote monitoring visits
• Drive the implementation of RBQM principles for high-quality execution of clinical trial activities
• Collaborate with site staff and cross-functional teams for efficient clinical trial execution

Clinical Research Associate, CRA

Compliance

• Shape the regulatory future of life-saving medicines
• Lead a global organization spanning four departments
• Oversee Chemistry, Manufacturing, and Controls (CMC) regulatory activities
• Ensure compliance while scaling manufacturing processes
• Develop approval strategies for new manufacturing sites
• Collaborate with supply chain and manufacturing teams
• Lead high-performing teams across multiple regions
• Manage negotiations with major regulatory bodies
• Ensure seamless transition as products move to large-scale manufacturing

Technical Supporter – New Filling Line, Maternity Cover

Manager, Clinical Operations

CNC Production Engineer I

GMP Material Professional

Clinical Research Associate

Global Associate Medical Director – Cardiovascular Disease

Director Stakeholder Engagement

Clinical Research Associate

Project Manager

Senior Operations Enablement Manager

Clinical Research Associate

Clinical Research Associate

Administrative Specialist

Clinical Research Associate, CRA

Senior Director, Regulatory Affairs – CMC and Lifecycle Management