At a Glance
- Tasks: Drive global regulatory disclosures and ensure compliance with evolving requirements.
- Company: Join Roche, a leader in healthcare innovation and transparency.
- Benefits: Inclusive culture, flexible working, and opportunities for personal and professional growth.
- Other info: Collaborative environment with a commitment to diversity and ethical practices.
- Why this job: Make a real impact on patient access to vital clinical information.
- Qualifications: Degree in Life Sciences and experience in regulatory affairs or project management.
The predicted salary is between 60000 - 75000 € 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.
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.
- 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.
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.
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 in Welwyn Garden City employer: F. Hoffmann-La Roche Gruppe
At Roche, we pride ourselves on fostering a culture of inclusivity and personal expression, where every employee is valued for their unique contributions. Our commitment to ethical practices in healthcare not only drives our mission to advance science but also creates an environment rich in collaboration and professional growth opportunities. Join us in a dynamic setting that encourages innovation and supports your career development while making a meaningful impact on global health.
Contact Detail:
F. Hoffmann-La Roche Gruppe Recruiting Team
StudySmarter Expert Advice🤫
We think this is how you could land Regulatory Transparency (Disclosures) Manager in Welwyn Garden City
✨Tip Number 1
Network like a pro! Reach out to current or former Roche employees on LinkedIn. A friendly chat can give you insider info about the company culture and the role, plus it shows your genuine interest.
✨Tip Number 2
Prepare for the interview by diving deep into Roche's mission and values. Be ready to discuss how your passion for regulatory transparency aligns with their goals. Show them you’re not just another candidate!
✨Tip Number 3
Practice your STAR technique for answering behavioural questions. Think of specific examples from your past that highlight your project management skills and ability to collaborate across teams. We want to see how you shine!
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets noticed. Plus, it shows you’re serious about joining the Roche family and contributing to a healthier future.
We think you need these skills to ace Regulatory Transparency (Disclosures) Manager in Welwyn Garden City
Some tips for your application 🫡
Be Yourself:At StudySmarter, we value authenticity. When writing your application, let your unique qualities shine through. Don’t be afraid to express your passion for transparency and how it aligns with our mission.
Tailor Your Application:Make sure to customise your application to highlight your experience in regulatory affairs and project management. We want to see how your skills can contribute to our goal of ensuring critical clinical trial data reaches the public.
Showcase Your Collaboration Skills:Since this role involves working across various teams, emphasise your ability to collaborate effectively. Share examples of how you've influenced cross-functional teams in the past, as this is key to thriving at Roche.
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 shows your initiative!
How to prepare for a job interview at F. Hoffmann-La Roche Gruppe
✨Know Your Stuff
Make sure you brush up on the latest global regulatory requirements and disclosure processes. Familiarise yourself with Roche's mission and values, especially around transparency in clinical trials. This will show that you're not just interested in the role, but also in how it fits into the bigger picture.
✨Showcase Your Experience
Prepare to discuss your previous experience in regulatory affairs or project management. Be ready to share specific examples of how you've influenced cross-functional teams or improved processes. This will demonstrate your ability to thrive in a dynamic environment and your commitment to quality and ethics.
✨Ask Thoughtful Questions
Come prepared with questions that reflect your understanding of the role and the company. Inquire about Roche's current initiatives in regulatory transparency or how they handle evolving global regulations. This shows your genuine interest and helps you assess if the company culture aligns with your values.
✨Be Yourself
Roche values personal expression and genuine connections, so don’t be afraid to let your personality shine through. Share your passion for healthcare and how you can contribute to their mission. Authenticity can set you apart from other candidates and help you connect with your interviewers.