Kerr Dental

Director

• Effectively execute and test the controls framework as per RCF (Risk and Controls Framework) methodology for HSE, BCM and NEM.
• Establishing and managing the HSE / BCM NEM Controls Framework, its design, implementation, execution, and continuous improvement.
• Ensuring transparent HSE, BCM & NEM Controls reporting is established for different organization levels, e.g. local, or unit level.
• Monitoring on an ongoing basis the business risk profile, considering for example organizational changes or changes in business model.
• Defining Control Entities in scope, supporting Control Entities in implementation of controls and remediation where needed.
• Providing Training to Control Entities.
• Managing the risk management process for HSE.
• Working closely and collaborating with other stakeholders like ERPC (Enterprise Risk, Policy and Controls), EPRM (External Partner Risk Management) etc. to ensuring close alignment and effective control governance & oversight.

Associate Director – Controls

Communications

• Set the vision and lead the global communications and engagement strategy for Corporate Affairs, delivering integrated programs that drive alignment, shape culture, and elevate functional performance
• Curate and deliver flagship engagement platforms—including global town halls, leadership forums, and initiatives that strengthen the talent pipeline and build deep connection to our purpose—ensuring leaders and teams are aligned on priorities and equipped to act
• Lead the function’s internal and external digital presence, ensuring a consistent, compelling narrative that supports strategic priorities, showcases functional excellence, and reinforces the company’s reputation
• Serve as strategic communications counsel to the Chief Corporate Affairs Officer and Corporate Affairs Leadership Team, developing high-impact messages and materials that inspire, influence, and mobilize key internal and external audiences
• Provide selective support for external speaking engagements and social media for the Chief Corporate Affairs Officer
• Partner across Corporate Affairs for Executive Committee communications alignment
• Convene and facilitate leadership briefings on priority topics, ensuring clarity, coordination, and timely decision-making across the global Corporate Affairs network
• Lead and support special projects that enhance functional performance, culture, and talent development, bringing structured execution and creative problem-solving to priority initiatives

Associate Director, Corporate Affairs Communications – Engagement

• Shape long-term capability strategy for Corporate Affairs
• Build and lead the Corporate Affairs Academy
• Develop high-impact learning experiences
• Manage digital content access
• Establish success metrics for capability development
• Curate internal and external thought leadership
• Elevate functional visibility and reputation

Director, Corporate Affairs Academy

Customer Success Manager

• Monitor clinical safety data, literature, and case reports to identify potential safety signals
• Conduct medical assessments for individual cases, including follow-ups and quality defect evaluations
• Perform signal detection and evaluation using aggregate and single-case data
• Contribute to regulatory responses and prepare safety data for health authority reviews
• Support safety input for core data sheets and related regulatory documentation
• Collaborate with cross-functional teams on clinical safety deliverables and study documentation

Medical Safety Lead – CRM

Medical Director

• Provide clinical leadership and medical strategic input for deliverables in the assigned project/program.
• Deliverables may include sections of individual protocols consistent with the clinical development plan (CDP), data review, program specific standards, clinical components of regulatory documents/registration dossiers, and publications (e.g., investigator brochures, briefing books, safety updates, submission dossiers, and responses to health authorities)
• Drive execution of the section of the program in partnership with global line functions, assigned Global Trial Directors, and regional/country medical associates
• Oversee/conduct medical and scientific review of trial data with Clinical Scientific Expert (CSE). May be the Program Manager of other associates (e.g.., CSE). May function as study medical monitor
• Support GPCH in ensuring overall safety of the molecule. May be a core member of the Safety Management Team, and supports program safety reporting (e.g., PSURs, DSURs, and safety related documents) in collaboration with Patient Safety
• Support the Clinical Development Head by providing medical input into CDP and clinical trial package reviews and contributing/driving development of disease clinical standards for disease areas
• Provide support to the GPCH or CDH in interactions with external partners (e.g., regulatory authorities, key opinion leaders, data monitoring boards, advisory boards, patient advocacy groups), internal partners (e.g., clinical trial team, Medical Affairs, Commercial, Health Economics & Outcomes Research), and decision boards)
• Work with BR (Novartis Biomedical Research)/Translational Medicine) to drive transition of early development projects to Transition Decision Point and with Business Development, including target identification and due diligences
• Ensure career development of Program Reports and clinical colleagues through active participation in performance management and talent planning processes. Provide on-boarding, training, & mentoring support
• Contribute to medical/scientific training of relevant Novartis stakeholders on the disease area and compound/molecule. May serve as speaker for Global Clinical team

Clinical Development Medical Director – Cardiology

Product Manager

• Develops and delivers winning HEOR strategy and tactics, with high quality and on-time availability
• Ensures that payer and healthcare needs are reflected into Phase 3b/4, RWE and integrated evidence plans
• Collaborates across divisions and functions to ensure effective integration of HEOR and payer evidence deliverables
• Partners closely with Regional and Country teams to design and oversee rollout of global HEOR and payer-evidence strategies
• Interacts with payers and relevant customer groups in priority countries

Director, HEOR Product Lead

Sales

• Responsible for business ownership of prescribing and referring physicians
• Driving relationships and creation and execution of business plans for territories
• Support product access and implement competitive response strategies
• Develop and employ customized tools and strategies for engaging with HCP targets
• Develop and execute a call-plan to achieve goals and improve access and sales opportunities

Radioligand Therapies Sales Specialist, Prostate

Account Executive

• Advise customers on Novartis’ product portfolio and services using digital and analog channels
• Analyze all available data sources and information and document insights about customers
• Use omnichannel customer engagement to maximize impact on patients, customers, and the company
• Responsible for territory and center management and for creating relevant territory, account, and customer contact plans
• Implement customer interaction concepts in cross-functional coordination with sales, medical, and key account management teams
• Develop product- and indication-related content, campaigns, and interaction plans in collaboration with teams

Sales Representative, Neurology - Multiple Sclerosis

Security Engineer

• Develop and enforce security policies and procedures related Digital Workspace across Novartis businesses to meet business and regulatory requirements
• Design security measures and overall Digital Workspace architecture for the IT landscape in line with the ISC policy framework
• Support and continually review technology standards and controls related to Digital Workspace and recommend information technology strategies, policies, and procedures
• Identify design problems within the Digital Workspace domain
• Support projects to evolve Digital Workspace solutions from evaluation to implementation and assist the delivery of the operational model
• Support the auditing of security policies and procedures
• Management communication with key stakeholders and provide reports to management
• Provide ongoing support to maintain the Digital Workspace domain’s effectiveness and efficiency by defining, delivering, and supporting strategic plans for implementing information technologies
• Develop and maintain relationships with key stakeholders and vendors
• Support the direction of technological research by learning the organizational goals, strategies and business drivers
• Develop and maintain architecture diagrams and documentation related to Digital Workspace processes and procedures
• Break down the strategic objectives to requirements on the solution portfolio and target architecture
• Key contributor on products, services and/or infrastructure strategies that require complex or advanced conceptualization
• Research and evaluate new Digital Workspace security technologies and make strategic security technology choices, directly supervising the quality of designs and implementation inside and between components
• Work with improvements, by participation in the development, of the architectural principles, processes, and standards.

Enterprise Security Architect – Digital Workspace

• Handle delivering sales performance and promoting product(s)
• Collaborate cross functionally in each geography as ONE team
• Develop and execute a call-plan to achieve goals and improve access
• Comfort in using sales data reporting tools to understand trends

Oncology Sales Specialist, Breast/Women’s Cancer

• Lead statistical programming activities for multiple clinical trials within a program or indication/disease area
• Accountable for timely and quality development and validation of all statistical programming components
• Responsible for audit readiness of all assigned programming deliverables
• Coordinate activities of internal/external programmers
• Make statistical programming decisions and propose strategies at program or indication/disease level
• Develop scientific documentation for the program or indication/disease area in collaboration with Biostatistician(s)
• Responsible for allocating resources within a program

Associate Director, Statistical Programming

Analyst

• Responsible for daily Novartis Patient Support Center (PSC) Workforce Management (WFM) operational execution
• Forecasting volumes in assigned queues
• Creating associate schedules based on forecasts
• Onboarding and off boarding of associates from WFM and applicable systems
• Monitoring attendance and the PTO system to ensure proper staffing levels
• Provide information to program management leadership on agent productivity and adherence

Analyst, PSC Workforce Management

Manager

• Delivery of complex or highly complex deliverables; responses to escalated medical enquiries for priority/launch brands
• Review of MI deliverables to ensure quality requirements are met
• Developing content for digital platforms
• Providing input into MI Service processes and standards to ensure optimal efficiency and productivity
• Management of Congress Medical Information booth enquiries
• Support (onsite, remote) to MI activities at congresses
• Reporting on enquiry metrics and insights from countries and regions

Senior Medical Information Manager

• Lead efforts to activate the new company-wide corporate narrative
• Ensure our purpose and values are communicated effectively across all audiences
• Design and implement a connected, multi-channel storytelling and thought-leadership approach
• Mobilize the Corporate Affairs organization as ambassadors for the narrative
• Oversee high-impact special communications projects critical to shaping and protecting the company’s reputation.

Executive Director, Corporate Narrative Activation – Special Projects

Account Manager

• Drive identification, implementation and scaling of strategic partnerships (data, academic, medical societies) and technology solutions (infrastructure, software, AI, data networks, federated platforms) to accelerate Real-World and clinical trial evidence aligned with business priorities.
• Execute innovative methodologies (e.g RWD to RCT linkage; implementation science; synthetic data) and digital tools to enhance evidence generation impact and scalability.
• Identify and recommend fit-for-purpose RWD based on hands-on assessment of relevance and reliability to address specific research questions that support product access and adoption.
• Translate evidence generation needs into fit-for-purpose requirements and relevant solutions in collaboration with cross-functional teams.
• Connect internal and external stakeholders to ensure consistent implementation of advanced solutions such as advanced statistical methods and ML/AI algorithms.
• Collaborate with research, academic, industry and startups partners to stay at the forefront of Evidence Generation innovation.
• Promote a culture of innovation to adopt novel scientific methods including pragmatic studies and hybrid trial models and creative ways to use data and technology solutions.
• Develop and communicate data and technology learning content and toolkits to support new evidence capabilities across global teams.
• Ensure partnered research meets regulatory, legal, and ethical standards while maintaining high data quality and integrity.