Novo Nordisk

Compliance

• own regulatory strategy and safety oversight for assigned products and projects
• lead regulatory submissions and approvals- prepare, product registrations and amendments, and respond to health authority queries
• ensure compliance and governance- maintain adherence to global and local regulatory standards, conduct reviews and audits, and manage compliance risks
• oversee pharmacovigilance activities: supervise collection, analysis and reporting of safety data, identify new safety signals and ensure timely regulatory reporting
• collaborate with stakeholders, partner with clinical, safety, commercial and external partners, and act as the company’s regulatory and safety contact for health authorities and policymakers
• monitor regulatory trends and adapt strategy, track regulatory changes, assess impact, and develop approaches to maintain compliance and accelerate approvals

Regulatory Affairs Lead – Levant

Learning and Development

• Deliver and execute leadership development priorities within assigned EVP/SVP areas
• Design and facilitate interventions using sparring, facilitation, coaching, and consultation
• Act as the primary point of contact for designated EVP areas or geographies
• Implement global processes, development offerings, and standards locally
• Collaborate with HR Business Partners and business leaders
• Lead innovation in leadership development by identifying, piloting, and scaling new learning approaches

Senior Global Leadership Development Manager

• Create and execute a 3-5-year strategic plan for your area, aligning functional objectives with affiliate, regional, and global direction.
• Together with your team develop and lead medical strategies for brands and pre-launch phases, ensuring proactive medical guidance to all functions.
• Develop strong network with key external stakeholders, including KOLs, Health Care professionals, Industry and patient associations, academic bodies, health authorities, NHS health boards and ABPI, aimed at fostering mutually beneficial partnerships and shaping market environment.
• Provide timely and relevant regulatory input enabling efficient product launches and marketing campaigns.
• Drive scientific communication strategies, including input to clinical trials, RWE plans, and publication strategies.
• Ensure compliance with ABPI Code of Practice, Health Authority requirements (MHRA) and the European Pharmacovigilance Framework.
• Lead, coach, and develop your direct reports and the whole team.
• Foster a diverse and inclusive work environment that allows people to give their best.
• Develop talents, ensuring succession planning, and participate in cross-functional development activities.
• Represent UK in internal Medical & Science regional and global leadership forums.

Senior Director, Medical & Regulatory

Research Analyst

• Realizar visitas de monitoreo (inicio, seguimiento y cierre) para asegurar el cumplimiento de los protocolos y regulaciones vigentes
• Verificar la integridad y exactitud de los datos fuente y su correcta transcripción en los cuadernos de recolección de datos electrónicos
• Garantizar la adherencia estricta a las normas ICH-GCP y a las regulaciones locales de ANMAT en los centros de investigación
• Gestionar y mantener actualizados los archivos maestros de ensayos electrónicos (eTMF) y sistemas IVRS
• Identificar y reportar hallazgos críticos o desviaciones al protocolo, proponiendo acciones correctivas inmediatas
• Actuar como el contacto principal entre el patrocinador y el centro de investigación para asegurar una comunicación fluida
• Coordinar la logística de suministros del estudio y el manejo de muestras biológicas bajo estándares de calidad

Clinical Research Associate, CRA

Product Specialist

• Identify and map key stakeholders within the assigned region to implement company marketing initiatives
• Engage regularly with doctors to promote company products, address queries, overcome objections, and secure prescriptions
• Meet sales effectiveness KPIs by achieving required call averages, frequency, coverage, personal order bookings, and related targets
• Ensure timely supply and availability of products by liaising with C&FA agents and stockists and placing necessary orders
• Conduct ongoing prescription audits and competitive analysis to track doctor engagement, evaluate previous visit outcomes, and monitor competitor activity
• Support strategic segmentation of doctors, assist in order booking, and provide feedback on market developments to sales leadership
• Collaborate with internal teams, organise approved educational activities, and maintain disciplined, timely reporting and administrative processes.

Marketing

• Support pre-launch activities for a MASH therapeutic asset
• Help coordinate creation and approval of digital marketing tactics
• Liaise with internal teams and agencies to track assets and timelines
• Assist with media planning and performance optimization
• Contribute to market research and stakeholder communications
• Participate in the program's capstone event, the Innovation in Action Case Competition

Intern - Liver Health

Program Manager

• Responsible for leading the Program Management and FRM teams and supports strategies that maximize access to therapies
• Responsible for driving best in class solutions while driving budget and program efficiencies
• Maintain a high-level of collaboration and integration with all relative field teams, Brand Marketing, Training, Market Access & Public Affairs, Trade, Legal, Compliance, Finance, HEOR, and Market Research
• Oversees existing patient support programs, manage team responsible for day to day operations with a focus on operational excellence in support of the patient journey
• Lead design, implementation and ongoing management of all programs
• Partner with analytics teams to develop performance dashboards and interpret operational data for purposes of assessing market access trends, hub program utilization, and performance against defined KPIs
• Function as subject matter expert on patient support solutions and collaborate cross functionally to design and implement programs that compliantly support the company’s patient support objectives for inline and launching brands
• Manage external partner performance against contractual arrangements, SOPs, KPIs, and budget. Ensure adherence to all compliance and regulatory requirements

Director, Program Management

Data Engineer

• Design and develop scalable data solutions by building robust applications and pipelines for data extraction, transformation, ingestion, and management that support analytics, reporting, and operational use cases
• Ensure high-quality and optimised data engineering processes by applying best practices, conducting testing and validation, and delivering solutions that meet reliability, scalability, and performance standards
• Provision data for analytics, AI, and ML by preparing, managing, and delivering high-quality datasets for traditional reporting, advanced analytics, AI/ML development, and broader business needs
• Collaborate with stakeholders across the organisation to understand business requirements, translate them into technical solutions, and deliver data products that support strategic and operational goals
• Drive technical excellence within the Data & ML Engineering area by representing the cluster in cross-functional settings, mentoring junior colleagues, and continuously improving engineering methods, techniques, and approaches

Senior Data Engineer

Data Scientist

• Convert complex commercial datasets into clear growth insights
• Deliver executive-ready recommendations with quantified impact
• Own commercial KPI frameworks and segment/cluster views
• Build and maintain advanced models to inform strategy
• Optimize omnichannel mix and budgets
• Lead competitor intelligence and scenario planning
• Mentor CRM professionals

CRM and Data Science Lead

People Operations

• Assist with various data-related projects and ad-hoc tasks.
• Support with data analysis, presentations and reporting.
• Collaborate with team members and stakeholders to deliver insights.
• Helping maintain data accuracy across HR systems.

Student Assistant, People Analytics

Director

• Serve as a member of NNRCC leadership team, contribute to NNRCC's strategy and goal setting.
• Lead and develop a highly professional, creative, engaging, energetic and respectful biomolecular technology team.
• Lead and develop an advanced biomolecular technology platform to enable NNRCC target discovery in cardiometabolic diseases and project progression upto G0 milestone.
• Ensure strategic fit and focus of NNRCC biomolecular technology team.
• Lead multifunctional work groups to carry out strategic and/or technology projects.
• Build and develop a strong network with internal and external stakeholders for collaboration and maximal value creation.

Director, Biomolecular Technologies

Product Manager

• Ensure strategic alignment with the overall product vision, objectives, and roadmap to drive team performance
• Apply evidence-informed discovery processes to validate user and business problems as well as potential solutions
• Define and monitor key product metrics and the team backlog to measure progress and guide future product decisions
• Build and maintain strong stakeholder relationships to align on priorities, manage trade-offs, and ensure continuous value realisation
• Stay up to date on digital product trends and technologies to enhance ways of working and maintain a competitive edge

Digital Product Manager

• Establish and lead a new, high‑impact team focused on next‑generation clinical data review and analytics across rare disease and CKAD portfolios.
• Drive strategic initiatives, build technical and reporting capabilities, and ensure delivery of robust, data‑driven insights that strengthen clinical quality, risk management and decision‑making across Development.
• Build and lead the Centralized Data Review team for Rare Disease and CKAD, setting targets, developing competencies and ensuring timely, high‑quality delivery.
• Lead large cross‑functional transformation programs (e.g., IQRMA), owning project delivery and translating complex clinical data topics into clear priorities for stakeholders.
• Establish a Centre of Excellence for data review reports, dashboards and visualisations, evaluating and implementing emerging technologies (including AI/ML) to enhance analytics.
• Ensure optimal resource allocation and operational performance by coordinating staffing, budgets and vendor engagement, and by monitoring deliverables and costs.
• Champion continuous improvement and quality by defining standards, sharing best practices, supporting audits, and promoting trustworthiness and compliance in clinical data handling.

Director, CDR, CKAD, RD & Transformation

• Develop and evolve a future Medical Affairs engagement model for obesity healthcare globally, including new types of obesity care providers
• Map and assess major international and national obesity healthcare providers
• Create and own a Global Medical Affairs engagement framework and strategy, including stakeholder mapping
• Contribute to the development of clinical care pathways and explore future treatment models
• Establish strong partnerships with obesity care providers in collaboration with cross-functional teams

Medical Director, Obesity Management and Digital Engagement

Account Manager

• 建立KA负责以外医院和公司长期战略合作伙伴关系
• 负责KA医院以外的GLP-1产品准入
• 负责目标医院当中，使已经列名产品不受到医院停药、限制等管理要求的限制(或好于预期的限制程度)，服务于患者
• 负责区域关键客户专家管理，并支持产品准入策略和专家的沟通和反馈
• 区域层面跨部门沟通，从而促进执