Novo Nordisk

Content Writer

• Be responsible for the preparation of complex aggregate safety reports, Risk Management Plans (RMPs), and responses to Health Authority questions
• Collaborate with cross-functional teams to ensure high-quality scientific writing and timely reporting of safety data
• Contribute to the evaluation and implementation of changes in local/global guidelines to ensure compliance with internal and external requirements
• Contribute to innovation and technical optimization projects within Safety Medical Writing to enhance efficiency, quality, and scalability of deliverables
• Drive process improvement activities, medical writing competency development and skill building across Safety Medical Writing.
• Act as an expert for junior team members, share information, and take proactive steps to excel in your role.

Safety Survey Medical Writing Specialist

Project Manager

• Lead end-to-end clinical trial delivery by planning, coordinating, and managing assigned clinical trials in line with protocols, regulatory requirements, GCP, and Novo Nordisk SOPs
• Drive cross-functional collaboration and communication by acting as the primary interface between HQ, CDC, regional teams, investigators, and external stakeholders
• Ensure operational excellence and compliance by overseeing trial execution quality, applying risk-based monitoring principles, and ensuring effective use of clinical systems
• Proactively identify, manage, and mitigate project risks by setting project-specific strategies, monitoring progress against milestones, and implementing mitigation plans
• Represent the CDC in key study forums and regulatory activities, including study meetings and investigator engagements, and ensuring timely support for local regulatory submissions

Engineer

• Create, draft, review, test and approve standard operating procedures to operate our new automated warehouse.
• Develop training materials in collaboration with the Training Project Manager to define needs.
• Collaborate with Denmark and other sites on standardization and documentation, including exchange workshops.
• Optimize processes and improve flows.
• Support new hires during onboarding and manage deviations during start-up.
• Contribute to operational readiness activities (Go-live preparation, readiness checklists, degraded-mode procedures and fallback scenarios).
• Work closely with automation, IT/OT and maintenance teams on operational processes related to AGV, WCS and SAP EWM systems.

Intra-logistics Engineer

Business Analyst

• Handling general accounting tasks such as posting incoming and outgoing payments, cash application, GL postings, invoicing, reconciliations, and performing month-end close activities.
• Providing high-quality support to affiliates in the Europe Markets Region.
• Acting as a sparring partner for the existing team in Finance GBS Bangalore to enhance knowledge about accounting processes.
• Fulfilling targets set by the Team Leader and GBS Finance Management.
• Working with key accounting processes such as reporting, review, reconciliation, and ad hoc analysis using SAP.
• Supporting the front office at affiliates and the Manager in Accounting GBS to achieve shared objectives.

Associate Business Analyst

Financial Planning and Analysis

• Handling general accounting tasks such as posting incoming and outgoing payments, cash application, GL postings, invoicing, reconciliations, and month-end close activities.
• Performing manual postings of incoming and outgoing payments and uploading postings from Excel to SAP.
• Managing bank reconciliations, including daily identification, research, and follow-up of payments, and clearing and reconciling IHB accounts using SAP.
• Processing intercompany transactions, ensuring reconciliation of accounts, and handling service fee invoices with proper documentation.
• Conducting month-end activities such as inventory reporting, depreciation posting, currency revaluation, and reporting the trial balance to the corporate accounting team.
• Ensuring compliance with Sarbanes-Oxley controls and preparing audit materials.

Associate II – Finance

Risk

• Ensure R&D excellence by designing and improving governance meetings
• Coach stakeholders like Global Project Leaders on decision criteria
• Plan and orchestrate governance interactions for timely project decisions
• Capture and follow up governance decisions and ensure closure
• Champion AI and digitalisation initiatives

Director, R&D Governance

Medical Director

• Ensuring Medical Affairs ambition, strategy, and tactics for the cardiometabolic therapeutic area align with short- and long-term BA WEST and corporate strategy
• Providing indirect medical leadership in BA WEST by offering strategic medical guidance and fostering strong medical networks
• Representing BA WEST in relevant regional and global teams, and external activities such as advisory boards and scientific associations
• Driving cross-functional collaboration and alignment of Medical Affairs activities with the overall strategic direction
• Leading external medical engagements with Key Opinion Leaders (KOLs) and other stakeholders to strengthen Novo Nordisk’s presence in the cardiometabolic therapeutic area
• Defining and executing on the scientific communication and publication strategy, including input to clinical trials, RWE plans, and patient-centered activities

Assoc. Cardiometabolic Medical Director

Compliance

• Lead regulatory affairs activities for assigned products in Australia and New Zealand, ensuring compliance while developing strategies to assist product development, registration, and commercialisation.
• Manage the preparation, compilation, and timely submission of accurate regulatory documentation for new product registrations, variations, renewals, and responses to queries.
• Serve as the primary liaison with regulatory authorities, maintaining positive relationships while monitoring and conveying developments in the regulatory landscape.
• Collaborate with cross-functional teams and stakeholders to provide regulatory guidance throughout the product lifecycle, represent regulatory affairs in decision-making processes, and assist with commercialisation.
• Maintain accurate regulatory records for assigned products in Regulatory Information Management (RIM) platforms, participate in audits to ensure compliance with regulatory standards, and contribute to updating and implementation of Standard Operating Procedures (SOPs) as needed.

Senior Regulatory Affairs Associate

Chief Marketing Officer

• Oversee commercial and medical strategies, brand positioning and marketing/sales activities in both HCP and consumer segments, ensuring effective execution of brand strategies.
• Monitor, analyze and act on market trends to identify emerging opportunities and inform commercial strategies.
• Develop and implement strategic marketing plans that align with the company’s goals, setting clear objectives and KPIs.
• Manage product/service development, collaborate on defining optimal pricing strategies to maximize profitability and competitiveness across channels.
• Lead impactful advertising campaigns and monitor sales performance, adapting strategies to drive performance.
• Develop and execute scientific communication strategies across clinical trial phases, integrating patient voices and providing input to clinical trials and Real-World Evidence (RWE) plans.
• Establish and maintain relationships with Key Opinion Leaders (KOLs) and facilitate collaboration and information exchange; organizing and conducting scientific meetings and symposia, delivering medical education to Healthcare Professionals (HCPs).

• Manage a team of 9 Finance Partners with broad FP&A responsibilities
• Drive value creation, finance partnering and insights for the R&D project pools
• Responsible for financial decision material and insights to drive efficient and value generating governance decisions
• Work with R&D Finance mgmt. team to continuously develop and strengthen how we work
• Process owner for the global clinical financial processes as well as all FP&A processes
• Responsible for standardization and optimization of processes and tools for the financial management of R&D project pools

Director, R&D Portfolio Finance

Account Manager

• Develop and lead strategic collaborations with pharmacy partners
• Act as the national point of contact for pharmacy relationships
• Design and execute a pharmacy partnership strategy
• Build and sustain long‑term relationships with pharmacies
• Create and implement promotional activities and disease‑awareness campaigns
• Work with internal stakeholders to integrate pharmacy initiatives
• Manage partner risk and compliance

Pharmacy Partnership Manager

Strategy

• Responsible for HEOR and real world strategy development, evidence generation and value communication
• Independently support the evidence generation strategy for a key product
• Act as a strategic partner with other senior leaders across commercial and medical functions in developing HEOR studies and programs using real world data, patient reported outcomes and modeling techniques
• Develop evidence plans and deliver studies and analyses to support the value proposition of Novo Nordisk product/s in the US market throughout the product lifecycle
• Play a role in overall vision and strategy of the department, coach and develop colleagues on specific areas of methodology and strategy
• Manage relationships and activities within the business unit and collaborate with all functions within HEOR, commercial and medical functions to develop and communicate evidence.

HEOR Evidence Strategy Director

• Act as the primary point of contact for health authorities and lead the hands-on preparation and coordination of meeting requests, responses, and commitments.
• Coordinate the collection of documents and lead the preparation of submissions for product approvals, including NCEs, post-approval variations, renewals, and import licenses.
• Maintain local processes for labelling and packaging compliance and conduct regulatory impact assessments for manufacturing and artwork changes.
• Support and ensure pharmacovigilance activities are processed in compliance with local regulations, including handling ICSRs, PSURs, and safety oversight on patient support programs.
• Partner with Quality, Supply Chain, and Commercial teams to translate regulatory requirements into actionable plans.

Assistant Manager, Regulatory

• Ensure products enter and remain on the market with compliant, commercially aligned claims, while meeting all internal and external regulatory requirements.
• Analyze regulatory issues and communicate effectively with key stakeholders, including global colleagues.
• Lead the preparation of regulatory documents, dossiers, and applications.
• Support the development of the strongest claims and promotion possible within the regulations.
• Actively contribute to high‑performing teams, including identifying ways to improve performance.
• Manage compliance within portfolio/activity streams.

Regulatory Affairs Manager

Data Scientist

• Design and develop production‑ready LLM/GenAI solutions for retrieval‑augmented generation (RAG), summarization and inference to address clinical and R&D use cases
• Build and integrate backend services, APIs and data pipelines (embeddings, vector DBs, knowledge bases) and support end‑to‑end deployment using cloud platforms and containerization
• Fine‑tune and evaluate models (supervised, LoRA/PEFT, prompt engineering), implement monitoring and testing frameworks for performance, fairness, hallucination rate, latency and cost
• Optimize models and systems (quantization, distillation, caching), and operationalise with LLM‑Ops tools and CI/CD best practices for stable, secure production use
• Ensure compliance with internal/external AI governance, data protection and regulatory requirements (anonymization, access controls, audit logging) and produce technical documentation and runbooks
• Collaborate with internal and external stakeholders across Data Science, Engineering, Medical and Regulatory teams to align on solutions, publish outcomes and drive technology roadmap adoption
• Stay current on LLM research, trends, best practices and technology roadmap, and pursue publications through R&D relevant activities