My work as License to Operate (LTO) Lead eases alignment between Medical and GxP Compliance, Healthcare Compliance, Group Legal Compliance, Risk Management, Access, Commercial & SHE to ensure our patients' safety. I proactively seek, influence and develop partnerships across Pharma International, Pharma Technical and Product Development functions to realise a cohesive horizontal LTO strategy and activity prioritisation. Key Roles in current position: - Co-Chair of the Affiliate LTO Forum-Cross-functional License to Operate Subject Matter Expert (SME) - Digital Workspace Automated Query Management (DWS AQM) International Patient Safety Change & Adoption Co-Lead - Product Owner for Senior Leader & General Manager LTO Onboarding in the Medical & GxP Compliance space - Affiliate Life Co-Product Owner In addition to these roles, I’m an active contributor to a number of internal networks within Roche advocating for diversity & inclusion and for patient partnership. Outside of work, I am committed to increasing patient outreach & involvement, through EUPATI and both the University Hospitals of Basel and Zürich as a Patient Research Partner.

Areas of Responsibility:• Effective resource planning and capacity evaluation, keeping a customer driven approach• Ensuring initiatives, processes and improvement activities impacting Local Quality and Local Safety ecosystems in countries are adequately prioritized• Developing tools and processes to enable Quality and Safety teams to readily identify what is critical at a country level, without putting the Licence to Operate at risk

Areas of Responsibility:• Global project, programme & change management expert (PROSCI, ITIL Foundation and Professional Scrum Master Certified)• Leading / facilitating major cross-functional strategic initiatives affecting 360+ staff in the Global HQ and 5000+ staff worldwide, across 80+ countries• Project management support for both Head of Medical Management Office and Head of PDMA Neuroscience Therapeutic Area, enabling smooth running of their teams, including budget, resourcing and vendor management and alignment across departments• Annual PDMA Leadership Team goal development and maintenance, enabling prioritisation and subsequent outcomes tracking across the full span of PDMA activities • Developing specialised internal communications, training & off-site meetings, including agenda development, key presentations, break-out sessions and workshops• Ensuring appropriate development and dissemination of guidance, tools, processes and best practices• Contributing to PD’s Agile Project Delivery CoP

Areas of Responsibility:• Providing project & change management and facilitation expertise for global and regional projects sponsored by the Head of Global Medical Affairs, international members of the Medical Affairs Council and the Regional Medical Directors• PM for transition of Project Symphony into business-as-usual• PM for European Medical CRM implementation

Areas of Responsibility:• Global Project Manager for pan-business Symphony Implementation (Separation of Commercial and Medical Activities within Pharmaceuticals Division, directly impacting 20,000 staff)• European Project Manager for Medical CRM Implementation and MSL Leadership Team, representing 800 Medical staff in 28 countries

Areas of Responsibility:• Translation of full scientific papers in the areas of medical research, engineering research and academic teaching

Areas of Responsibility:• Accountable for managing the Engagement Process to improve overall Delivery Excellence by driving the globally consistent use of the GBS CRM Process• Collaboration with the key stakeholders in Opportunity Management, Pricing, Procurement, Business Control, Audit and others in change management, reporting and issue resolution• Provided guidance and hands-on support to the Geographical and Integrated Operating Teams to drive a stronger understanding of Engagement Process to ensure both compliance needs and business objectives were met

Areas of Responsibility:• Variety of client-facing management roles for global multi-language organisations including:• Global Operational Change Team Lead• Training and Coaching Lead• Lead Business Requirements Analyst• Global DOCUMENTUM Business Consultant• EDRMS Subject Matter Expert• Requirements gathering and business analysis• Developing and implementing systems to support document authoring, review, and publishing in regulatory submissions • Integration of global processes for New Drug Development and Pre-Clinical Research, ensuring these global systems were validated and compliant with US electronic signatures regulation (21 CFR Part 11) and other applicable regulations

Areas of Responsibility:• Variety of client-facing management roles for global multi-language organisations including:• Global Operational Change Team Lead• Training and Coaching Lead• Lead Business Requirements Analyst• Global DOCUMENTUM Business Consultant• EDRMS Subject Matter Expert• Requirements gathering and business analysis• Developing and implementing systems to support document authoring, review, and publishing in regulatory submissions • Integration of global processes for New Drug Development and Pre-Clinical Research, ensuring these global systems were validated and compliant with US electronic signatures regulation (21 CFR Part 11) and other applicable regulations

Areas of Responsibility:• Project and programme management• Business case development and benefits identification• Risk & issue management• Management of initiatives as an integrated portfolio to optimise business benefits• Valuation of individual projects in the programme portfolio against the benefits they will yield• Strategic prioritisation and allocation of resources

Areas of Responsibility:• Member of the Research Directorate, covering a portfolio of five therapeutic areas with ~200 staff, leading the project planning, resource assignment and management information service for Healthcare and Drug Delivery R&D projects from their inception to product launch• Supervised the development of project and programme plans, coupled with monitoring and reporting on project progress, resource requirements and resource utilisation during the project lifecycle• Advised on the viability of individual projects and their portfolio fit, recommending hiring / retraining strategies

Areas of Responsibility:• Defined ERP software enhancement for pharmaceutical, medical & surgical products supply chain reorganisation• Evaluated country-specific business requirements • Identified local best practices and managed their incorporation into the business-wide transformation process

Areas of Responsibility:• Drove development projects and ideas for future research, ensuring the successful transition from Research to Production (scale-up and technology transfer)• Acquired solid working knowledge of ISO 9001, GLP, GMP and GCP applied to R&D and Process Development (including the development of new technologies and working practices and their scale-up into production)• Project Leader for major wound management projects (23 FTE across three sites, from biological sciences and clinical trials to manufacturing, marketing and sales)• Responsible for managing the evaluation, planning, and coordination of project activities and departmental studies, including pre-clinical and clinical trials, ensuring their scientific content and accuracy