Regulatory Disclosures Professional (Manager)

Roche; England; On-site; GBP 60,000 - 80,000; Full time

Job summary

A global healthcare company is seeking a Regulatory Affairs professional to ensure compliance with global disclosure requirements. You will lead efforts to register clinical trials and collaborate with cross-functional teams. The ideal candidate has a degree in Life Sciences and extensive experience in regulatory affairs, demonstrating strong project management skills and fluency in English. Join us in making a global impact by advancing healthcare solutions.

Benefits

Flexible working environment

Qualifications

• Several years of experience in a scientific or regulatory environment.
• Ability to influence and collaborate effectively across teams.
• Strong written and verbal communication skills.

Responsibilities

• Provide expert regulatory guidance for global disclosure requirements.
• Drive posting of clinical trial protocols to public registries.
• Lead initiatives to optimize information flow across functions.

Skills

Project management expertise

Regulatory affairs knowledge

Fluency in English

Collaboration across teams

Attention to detail

Education

Degree in Life Sciences or equivalent

Job description

Are you passionate about transparency and ensuring critical clinical trial data reaches the public? Join the Product Development Regulatory Affairs (PDR) Data and Content Chapter, where you will drive the strategy and execution of global regulatory disclosures. This is an opportunity to play a pivotal role in upholding Roche's ethical commitments and shaping how patients, healthcare professionals, and the scientific community access vital clinical information.

You will ensure compliance with evolving global disclosure requirements while protecting sensitive information, contributing directly to Roche's mission to deliver meaningful medical advances for patients worldwide.

Responsibilities

• Ensure strategic compliance: Provide expert regulatory guidance to ensure Roche meets global disclosure requirements while safeguarding Personal Protected Data and Company Confidential Information
• Lead global trial registration: Drive the accurate and timely posting of clinical trial protocols and study results to public registries such as ClinicalTrials.gov and the EU results registry
• Enhance process excellence: Lead cross‑functional initiatives to optimize information and process flow, translating business needs into efficient, globally aligned system enhancements
• Mentor and influence: Act as a Global or Business Process Owner and Subject Matter Expert, mentoring colleagues and helping to shape the internal and external environment for regulatory transparency
• Collaborate across functions: Partner with project teams, affiliates and other cross‑functional stakeholders to secure data, coordinate reviews and ensure high‑quality and consistent disclosure deliverables
• Shape regulatory transparency: Contribute to internal and external efforts to advance Roche's leadership in regulatory transparency, maintaining awareness of emerging global requirements and trends

You are a proactive and detail‑oriented professional who thrives in a dynamic, matrix‑based environment. You demonstrate sound judgment, a commitment to quality and ethics, and the ability to manage complex projects across multiple stakeholders.

Qualifications

• Strong and proven experience, including several years supporting cross‑functional teams in a scientific or regulatory environment
• Degree in Life Sciences or equivalent
• Demonstrated project management expertise, with exceptional attention to detail and the ability to deliver high‑quality work under challenging timelines
• Proven ability to influence and collaborate effectively across global, cross‑functional teams
• Excellent written and verbal communication skills, with fluency in English
• Extensive experience in regulatory affairs or other product development functions, and a deep understanding of global regulations, disclosure processes and drug/biologics development (including GxP and GCP) is preferred

A 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.