LTO Regulatory Partner - 12 month Fixed Term Contract

F. Hoffmann-La Roche AG; Welwyn Garden City; Hybrid; GBP 45,000 - 60,000; Full time

Job summary

A leading pharmaceutical company in Welwyn Garden City seeks an LTO Regulatory Partner for a 12-month fixed term contract. The role focuses on leveraging regulatory expertise to influence patient outcomes, managing UK clinical trial applications, and collaborating cross-functionally to ensure compliance with UK regulations. Ideal candidates will possess at least a scientific degree, relevant regulatory experience, and strong documentation skills. Enjoy a hybrid work environment with flexible options.

Qualifications

• Basic experience in UK Regulatory Affairs.
• Proven experience managing UK clinical trial applications.
• Knowledge of UK and EU regulatory requirements.

Responsibilities

• Leverage regulatory expertise for strategic initiatives.
• Collaborate to translate regulatory requirements into Roche policies.
• Manage UK clinical trial applications and provide strategic advice.

Skills

Regulatory knowledge

Stakeholder management

Documentation skills

Collaboration

Agile mindset

Education

Scientific University degree

Job description

LTO Regulatory Partner - 12 month Fixed Term Contract page is loaded## LTO Regulatory Partner - 12 month Fixed Term Contractlocations: Welwyntime type: Tempo integralposted on: Publicado hojetime left to apply: Data de término: 10 de janeiro de 2026 (23 dias restantes para se candidatar)job requisition id: 202512-131602At 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**A healthier future. It’s what drives us to innovate. To continuously advance science and ensure everyone has access to the healthcare they need today and for generations to come. Creating a world where we all have more time with the people we love.****The Opportunity******Location:** Welwyn Garden City (Hybrid - 2 days per week on-site)******Duration:** 12-Month FTC****Imagine working for an organization that puts people at the heart of everything they do, where your contributions directly impact patient outcomes. At Roche, our number one priority is our patients, and we believe that every person plays a key role in achieving this mission.****As a Regulatory Partner at Roche UK, you will be a vital part of our UK Regulatory Chapter. You will leverage your regulatory and scientific expertise to shape and drive strategic initiatives. This is your opportunity to make a difference and be part of a company dedicated to improving lives.****UK Regulatory Chapter Responsibilities****The Regulatory group collaborates with the wider business to translate the constantly evolving requirements of the UK regulatory environment into Roche policies, procedures, solutions, and strategies that ensure compliance and maximize the value for patients.****Our activities encompass:*** **Clinical Trial Applications*** **National Licensing Applications*** **Early Access to Medicines Applications*** **National components of medicines authorisation via the European Centralised procedure****The team serves as Roche's primary contact with the MHRA, requiring effective cross-functional collaboration at both local and global levels, as well as the capability to negotiate and influence externally. Regulatory Partners need to be adaptable and entrepreneurial to identify opportunities, while maintaining a focused approach on ensuring compliance and playing a key role in retaining Roche UK's License to Operate.****Who You Are****You are a passionate regulatory professional with a clear vision for improving patient outcomes. You have an agile mindset with a collaborative, solution-oriented approach.****With a good understanding of the pharmaceutical industry and some experience working within a regulated environment, you will leverage your regulatory knowledge and experience to deliver on foundation work and support with chapter and/or squad work. You may contribute to the development of squad/chapter-based strategic plans and goals. You will have the ability to understand scientific and technical information relating to an assigned portfolio of Roche products.****You also bring:*** **A Scientific University degree*** **Basic experience in UK Regulatory Affairs*** **Proven experience managing UK clinical trial applications*** **Experience providing strategic and technical advice*** **Knowledge and experience of UK and EU regulatory requirements and procedures*** **Excellent documentation skills to ensure high-quality and timely submissions*** **Experience as a Subject Matter Expert (SME) in defined subject areas or therapeutic areas*** **Experience managing stakeholder relationships**### Who we areA healthier future drives us to innovate. Together, more than 100’000 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 life-changing healthcare solutions that make a global impact.Let’s build a healthier future, together.The statements herein are intended to describe the general nature and level of work being performed by employees, and are not to be construed as an exhaustive list of responsibilities, duties, and skills required of personnel so classified. Furthermore, they do not establish a contract for employment and are subject to change at the discretion of Roche Products Ltd. At Roche Products we believe diversity drives innovation and we are committed to building a diverse and flexible working environment. All qualified applicants will receive consideration for employment without regard to race, religion or belief, sex, gender reassignment, sexual orientation, marriage and civil partnership, pregnancy and maternity, disability or age. We recognise the importance of flexible working and will review all applicants’ requests with care. At Roche difference is valued and we are proud to be an equal opportunity employer where you are encouraged to bring your whole self to work.