At a Glance
- Tasks: Ensure compliance with global disclosure requirements and lead clinical trial registrations.
- Company: Join Roche, a leader in healthcare innovation and diversity.
- Benefits: Flexible working environment, competitive salary, and opportunities for personal growth.
- Other info: Collaborative culture that values diversity and encourages personal expression.
- Why this job: Make a real impact on global healthcare while shaping regulatory transparency.
- Qualifications: Degree in Life Sciences and experience in regulatory affairs or project management.
The predicted salary is between 60000 - 80000 £ per year.
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
- 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.
Who you are
- 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.
- 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.
Who we are
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.
Regulatory Transparency (Disclosures) Manager employer: F. Hoffmann-La Roche AG
Contact Detail:
F. Hoffmann-La Roche AG Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Regulatory Transparency (Disclosures) Manager
✨Tip Number 1
Network like a pro! Reach out to people in the industry, especially those at Roche. A friendly chat can open doors that a CV just can't.
✨Tip Number 2
Prepare for interviews by knowing your stuff! Research Roche’s values and recent projects. Show them you’re not just another candidate, but someone who truly gets their mission.
✨Tip Number 3
Practice makes perfect! Do mock interviews with friends or use online resources. The more comfortable you are, the better you'll shine when it counts.
✨Tip Number 4
Apply through our website! It’s the best way to ensure your application gets seen. Plus, you’ll be part of the Roche community from the get-go!
We think you need these skills to ace Regulatory Transparency (Disclosures) Manager
Some tips for your application 🫡
Tailor Your Application: Make sure to customise your CV and cover letter for the Regulatory Transparency (Disclosures) Manager role. Highlight your relevant experience in regulatory affairs and project management, showing us how you can contribute to Roche's mission.
Showcase Your Skills: Don’t hold back on showcasing your written and verbal communication skills. We want to see how you can effectively convey complex information, especially in a cross-functional environment. Use examples that demonstrate your ability to influence and collaborate.
Be Detail-Oriented: Attention to detail is key in this role. Make sure your application is free from typos and errors. We appreciate candidates who take the time to ensure their submissions are polished and professional.
Apply Through Our Website: We encourage you to apply directly through our website. It’s the best way for us to receive your application and ensures you’re considered for the role. Plus, it gives you a chance to explore more about Roche and our values!
How to prepare for a job interview at F. Hoffmann-La Roche AG
✨Know Your Regulatory Stuff
Make sure you brush up on global disclosure requirements and regulations relevant to the role. Being able to discuss specific regulations and how they impact Roche's operations will show that you're not just familiar with the basics, but that you’re genuinely invested in the field.
✨Showcase Your Project Management Skills
Prepare examples of past projects where you successfully managed complex tasks across multiple stakeholders. Highlight your attention to detail and how you ensured high-quality outcomes under tight deadlines. This will demonstrate your capability to thrive in a dynamic environment.
✨Emphasise Collaboration
Roche values teamwork, so be ready to share experiences where you collaborated effectively with cross-functional teams. Discuss how you influenced others and contributed to achieving common goals, as this aligns perfectly with the role’s requirements.
✨Communicate Clearly and Confidently
Since excellent communication skills are crucial for this position, practice articulating your thoughts clearly. Be prepared to explain complex regulatory concepts in simple terms, showcasing your ability to mentor and guide others in the process.