At Roche you can show up as yourself embraced for the unique qualities you bring. Our culture encourages personal expression open dialogue and genuine connections where you are valued accepted and respected for who you are allowing you to thrive both personally and professionally. This is how we aim to prevent stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche where every voice matters.

The Position

About Roche Product Development Regulatory (PDR)

We are a flexible bold and distinctive regulatory organization. We make decisions quickly and strategically as the environment & landscape evolves. We innovate. Our communities form a culture where I YOU and WE learn continuously. We deliver insights to the Roche organization. We apply these insights to develop our portfolio effectively and efficiently. We employ our unique strengths through a strong sense of purpose to create medical advances for society. We thrive as a community while enjoying fulfilling work and meaningful careers. We trust and rely on each other. We try new approaches. We openly discuss and learn from our mistakes and our failures. We experiment and iterate to achieve our aspirations. I YOU and WE feel pride in the impact we make together for patients.

About this Chapter in PDR
The PD Regulatory Program Management Chapter is accountable and responsible for delivering global regulatory strategy and end to end of clinical projects in the Roche portfolio in order to develop and maintain Roche product licenses to meet the needs of our patients. Chapter members deliver the regulatory components of clinical development and registration programmes for products both preand post licensing. Chapter members do this by developing innovative and effective global regulatory strategies assessments and plans and supporting documentation in collaboration with regional regulatory affairs counterparts cross functional product teams corporate partners and global health authorities based on uptotheminute regulatory knowledge and expertise. Chapter members lead and support global Health Authority interactions and procedures represent regulatory affairs on crossfunctional project teams and ensure the consistent and safe use of our medicines through highquality labels.

This Job is a Leader position. A Leader in PDR has a broad understanding of the regulatory landscape and applies their knowledge in the of deliverables aligned with our True North. Our leaders are accountable for advocating and driving changes throughout the organization and support our people in a matrixed environment. With a thorough understanding of priorities and areas of high impact PDR leaders connect the right people and resources with the right work and help the organization adapt to evolving regulatory requirements. You will inspire all of our people to boldly innovate collaborate and create outcomes that matter for patients stakeholders and the company. To maintain our License to Operate in a highly regulated industry medical compliance and adherence to the Roche Group Code of Conduct are every employees responsibility. This includes ensuring that you have the appropriate training experience and qualifications necessary to perform and complete your work in accordance with regulatory requirements and corporate policies and standards.

All leaders have a role in supporting the PDR vision statement. Regulatory Leaders will:

• closely partner with the PDR Community and relevant stakeholders to build an agile network of empowered individuals

• foster an environment of trust where individuals can openly share thoughts ideas and feedback with each other and team/community impact discussions are essential

• actively enable people to take ownership of their professional and personal development

• role model the shared sense of purpose across PDR

• openly share successes and failures to encourage learning

• lead with a creative mindset and according to VACC (Visionary Architect Coach Catalyst) principles

• build an environment in which all community members can thrive

Purpose
Together with the Portfolio Data and Content Lead and in collaboration the Portfolio Team coleads supports delivery of the regulatory portfolio according to enterprise and PDR priorities:

• Has oversight of the regulatory strategy risk mitigation and HA interactions at the entire portfolio level

• Contextualizes internal and external regulatory developments in order to ensure that PDR skill sets capabilities investment strategies relationships and portfolio priorities are adequate to deliver the evolving portfolio in line with the PDR Moonshots and True North

• Acts as a senior advisor and key stakeholder to Portfolio Team CoLeads who are accountable and responsible for setting and executing the regulatory and content strategy for a portfolio of products

Job Expectations and Key Accountabilities:

• This individual is viewed as a scientific regulatory expert and strategic thought leader who can balance moving forward regulatory strategies for innovative solutions with the need to maintain our license to operate. They will be a scientific regulatory expert and key influencer at internal Roche leadership teams strategic enterprise initiatives and governance bodies

• Identifies and interprets regulatory trends to build enterprise insights so that the organization can assess and adjust if necessary. As a subject matter expert in regulatory strategy contributes to the generation of regulatory knowledge and insights ensuring these are shared within PDR and with stakeholders. If needed catalyzes change

• Accountable to input into the prioritization of deliverables as defined by the PDR One Enabling team and Area 2 teams and ensures prioritized work packages are understood by the portfolio teams

• Ensures Portfolio Team Leads and portfolio team members have the necessary overall business context and direction to be empowered for creating and executing strategy and HA interactions for products within the portfolio

• Brings a holistic portfolio overview to the Portfolio Team Leads Network sharing knowledge insights and prioritization with the Portfolio Team coleads to ensure clear understanding and alignment on the priorities set by the PDR One Enabling team and Area 2 decision making

• Together with the Portfolio Data and Content Lead and Portfolio Team coleads is responsible for establishing ways of working and effectiveness of the Portfolio Teams; as well as ensuring the necessary expertise and resources are available to deliver the work and foster growth and development of the team

• Supports talent flow within into and out of the Portfolio Teams

• Builds an implementable and robust succession plan for future Portfolio Strategy Leads

• Acts as an advisor/consultant to any member of PDR or the wider organization

• Accountable for building partnerships with senior key stakeholders from other functions to ensure the strategic business goals are met through the sharing of knowledge expertise and the provision of appropriate resources

• Accountable for stakeholder management within and outside of PDR including alignment prioritization issue escalation and conflict

• Accountable for building working relationships with key Health Authorities according to the chapter stakeholder map

• Accountable for collaborating with and influencing industry associations and Health Authorities on key portfolio and regulatory policy matters

• May have direct reports

• May dedicate a percentage of their time to the Chapter Squads PDR projects and/or enterprise initiatives

Job Experience and Knowledge:

• Demonstrated leadership in drug development global regulatory strategy and for a variety of products

• Experienced in managing and interacting with internal and external stakeholders

• Experienced in leading a high performing team

• 15 years of relevant experience including a minimum of 12 years supporting crossfunctional teams in a scientific environment

• Regulatory and drug development experience across multiple therapeutic areas (Oncology Neurology Ophthalmology Cardiovascular Renal Metabolic Immunology)

• Knowledge of manufacturing regulatory as well as device regulations with proven ability to influence and navigate the broader regulatory strategy behind the development strategies

• Proven track record navigating highly complex projects as well as corporate critical activities enabling business continuity

• Trusted enterprise leader who can lead initiatives on behalf of the Corporate Executive Committed Pharma Leadership Team Research & Early Development organizations in Roche Group (REDs) and Pharma Development Leadership Team

• External crossstakeholder engagement (e.g. working groups peerreviewed publications presentations at meetings) to advance innovation in regulatory science

Who we are

A healthier future drives us to innovate. Together more than 100000 employees across the globe are dedicated to advance science ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities foster creativity and keep our ambitions high so we can deliver lifechanging healthcare solutions that make a global impact.

Lets build a healthier future together.

Basel is the headquarters of the Roche Group and one of its most important centres of pharmaceutical research. Over 10700 employees from over 100 countries come together at our Basel/Kaiseraugst site which is one of Roches largest sites. Read more.

Besides extensive development and training opportunities we offer flexible working options 18 weeks of maternity leave and 10 weeks of gender independent partnership leave. Our employees also benefit from multiple services on site such as childcare facilities medical services restaurants and cafeterias as well as various employee events.