Novartis

AI Engineer

• Oversee a centralized, multi-tenant data hub enabling countries to collaborate, share, and co-create data assets to drive the industrialization of analytics and AI.
• Define and implement the AI strategy for SAP systems aligned with enterprise architecture and business goals.
• Identify opportunities for AI-driven innovation within SAP processes.
• Collaborate with SAP functional and technical teams to embed AI into workflows and applications.
• Establish AI governance frameworks for SAP environments, ensuring compliance with data privacy and ethical AI standards.
• Define implementation strategy for seamless integration of AI solutions with SAP systems and external data sources.
• Develop road maps describing the evolution for the functional Domain of all enterprise solution portfolios from current state to future state.

Director – Automation and AI Architect

Director

• Lead the development and execution of the medical affairs strategy for assigned therapeutic areas and assets.
• Co-develop integrated evidence plans, including interventional and non-interventional studies, real-world evidence (RWE), and implementation science.
• Collaborate with Medical Science Liaisons (MSLs), Field Medical teams, and external stakeholders to deliver high-impact medical education and scientific communication.
• Represent GMA in cross-functional forums, including regulatory, commercial, and development teams.
• Provide strategic input into reimbursement and market access strategies.
• Ensure compliance with internal policies and external regulatory standards.
• Act as a subject matter expert and provide leadership in complex scientific and regulatory environments.

Director, Global Medical Affairs – Neuroscience

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

• Lead statistical programming activities for multiple clinical trials within a program or an indication /disease area, or development program.
• Accountable for timely and quality development and validation of all statistical programming components on assigned program(s).
• Responsible for audit readiness of all assigned statistical programming deliverables as well as accuracy and reliability of statistical analysis results.
• 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(s) or indication/disease area together with the Biostatistician(s).
• Responsible for allocating resources within a program and ensuring resource sharing between programs to meet AQS and organizational goals.
• May act as an operational and/or functional manager of associates including providing supervision and guidance to these programmers on operational / functional expertise and processes.
• Recruit, mentor, and develop statistical programmers.
• Build and maintain effective working relationships with cross-functional team members within the clinical trial/program, and able to summarize and discuss status of deliverables and critical programming aspects with them (timelines, scope, resource plan).
• Maintain up-to-date advanced knowledge of programming software (e.g. SAS/R) as well as industry requirements (e.g. CDISC, eCTD, Define.xml), attend functional meetings and training.
• Represent statistical programming at indication or program-level, in audits/inspections and Health Authority (HA) meetings, and on technical programming aspects in external conferences or consortiums (e.g. CDISC).

Associate Director, Statistical Programming

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

• Work closely with Therapy Area teams, key markets and functions to ensure our patient strategy for priority diseases is driven by insights and supported by high quality content, channels, and solutions that enhance the patient experience.
• Raise standards and consistency of execution through applying the International Patient Excellence (IPEx) framework to priority disease areas and brands.
• Work with Therapeutic Area teams and key markets to co-create patient-focused content and solutions that meet organizational and patient needs.
• Use the IPEx 5R framework to consistently guide personalized patient solutions, content and experience journeys.
• Deliver high-impact, patient-focused content across all channels.

Director, Patient Experience and Activation

Analyst

• responsible for meeting their monthly performance measurements and delivering on their assigned responsibilities
• responsible for forecasting volumes in assigned queues
• creating associate schedules based on forecasts
• plotting associates into schedules
• onboarding and offboarding of associates from WFM and applicable systems
• overseeing time off tracking and attendance adherence
• performing analysis whenever service levels are at risk
• providing clear root cause analysis of any service level misses
• monitoring attendance and the PTO system to ensure proper staffing levels
• oversee holiday schedule management
• providing information to program management leadership on agent productivity and adherence
• identifying opportunities for innovative automation, workload balancing, queue management, and process changes to increase predictability of the PSC’s ability to meet objectives and goals

Analyst, PSC Workforce Management

Affiliate Manager

• Leading of the Baltic regional Pipeline group
• Accountable for coordinating of x-functional team- medics, V&A, HEOR, commercial, finance, regulatory
• Runs regular touchpoints and cascade of information of the situation mapping of the reimbursement landscape, unmet need, clinical data and regulatory update, competitor overview, strategic choice and recommendation of pipeline GtM strategy building up to -12 month before EU MA
• Works very closely with the Baltic regional medical SPOC for insight generation, unmet need identification, treatment pathways and gap identifications, clinical data and progress and identification of evidence gaps.
• Generates in cooperation with finance team and local commercial teams assets forecasts, based on patients funnel, global recommendation and localisation
• Ensures LT sign off of pipeline GtM strategies and recommendations
• Responsible for early V&A insight external generation
• Accountable for V&A regional dashboard of pipeline and regular communications
• Achieving optimal national patient access outcomes.

New Products – Strategic Partner

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 IDP, data review, program specific standards, clinical components of regulatory documents/registration dossiers, and publications (e.g., IBs, 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 (GTDs), and regional/country medical associates.
• Oversee/conduct medical and scientific review of trial data with Clinical Scientific Expert(s).
• May be the Program Manager of other associates (e.g., CSE).
• May function as study medical monitor.
• Support SR/GPCH in ensuring overall safety of the molecule.
• May be a core member of the Safety Management Team (SMT), and supports program safety reporting (e.g., PSURs, DSURs, and safety related documents) in collaboration with Patient Safety.
• Support the Therapeutic Area Head (TAH) by providing medical input into IDP and CTP reviews and contributing/driving development of disease clinical standards for disease areas.
• Provide support to the (Sr.) GPCH or TAH in interactions with external partners (e.g., regulatory authorities, KOLs, data monitoring boards, AD Boards, patient advocacy groups), internal partners (e.g., CTT, Research, Translational Medicine, GMA, Marketing, HE&OR), and decision boards.
• Work with BR (Biomedical Research)/Translational Medical Sciences) to drive transition of pre-PoC projects to DDP and with BD&L including target identification and due diligences together with additional matters.
• 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 franchise.
• May serve on or lead global initiatives (e.g., process improvement, training, SOP development, other Clinical Development line function initiatives).

Clinical Development Medical Director – Cardiovascular

• Providing clinical leadership and strategic input for all clinical deliverables in the assigned project or section of a clinical program. Clinical deliverables may include clinical sections of individual protocols or sub studies consistent with the Integrated Development Plans (IDP), clinical data review, program specific standards, clinical components of regulatory documents/registration dossiers, and publications
• Leading development of clinical sections of trial and program level regulatory documents
• Driving execution of the section of the clinical program in partnership with global line functions, assigned Global Trial Directors (GTDs), and regional/country medical associates, if applicable
• Overseeing/conducting ongoing medical and scientific review of clinical trial data with Clinical Scientific Expert(s) with appropriate oversight from Medical Lead
• Supporting (Sr.) GPCH in ensuring overall safety of the molecule for the assigned section and may be a core member of the Safety Management Team, supporting overall program safety reporting in collaboration with Patient Safety
• As a clinical expert, supporting the (Sr.) GPCH or CDH in interactions with external and internal stakeholders and decision boards
• Contributing to scientific training of relevant Novartis stakeholders on the disease area and compound/molecule. May serve as speaker for franchise medical/scientific training and may be the Program Manager of other associates.

Senior Clinical Development Director – CV

• Lead efforts to activate the new company-wide corporate narrative
• 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 company’s reputation

Executive Director, Corporate Narrative Activation – Special Projects

Sales

• Drive demand creation and develop, coordinate, and implement strategic business plans focused on referral and treatment networks
• Responsible for business ownership of prescribing and referring physicians
• Support product access and implement competitive response strategies
• Develop and employ customized tools and strategies to gain access to engage with HCP targets
• Comfort in using sales data reporting tools to understand trends and identify growth opportunities
• Exhibit strong self-awareness, ability to inspire, and willingness to challenge the status-quo