At a Glance
- Tasks: Support global compliance by managing clinical trial disclosures and ensuring timely posting of information.
- Company: Join Roche, a leader in healthcare innovation with a culture that values diversity and personal expression.
- Benefits: Flexible working environment, competitive salary, and opportunities for professional growth.
- Other info: Collaborative team environment with a focus on trust and excellence.
- Why this job: Make a real impact on healthcare by accelerating medical advances through regulatory transparency.
- Qualifications: Degree in Life Sciences, attention to detail, and experience in regulatory affairs preferred.
The predicted salary is between 40000 - 50000 € 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.
In Product Development Regulatory Affairs (PDR), we are a flexible, bold, and distinctive regulatory organization that innovates quickly to make a meaningful impact for patients. You will join the PD Regulatory Data and Content Chapter, a community that drives the end‑to‑end strategy, generation, and execution of content and data to support the entire Roche portfolio, ensuring we deliver high‑quality, impactful submissions to global Health Authorities.
As a Regulatory Disclosure Specialist, you will play a critical role in supporting global compliance and transparency by assisting with the public disclosure of Roche's clinical trial information. This rewarding role offers a chance to apply your attention to detail and organizational skills to help accelerate medical advances for society.
- Assist in the accurate and timely posting of applicable clinical trial protocols and study results to public websites and the EU results registry.
- Support the coordination of disclosure workflows, helping to identify required studies and timelines, and tracking progress from initiation to completion.
- Collaborate with project teams, affiliates, and cross‑functional partners to ensure alignment on regulatory disclosure requirements.
- Contribute to the submission and quality control of protocol documents, ensuring consistency between registry entries and the final protocol.
- Help drive functional excellence within Regulatory Disclosures by applying process and project management skills, supporting a culture of trust and collaboration.
You are a detail‑oriented team player who thrives in a global, matrix‑based environment. You have a strong sense of responsibility, high ethical standards, and the ability to deliver quality work under tight timelines.
- Degree in Life Sciences or equivalent.
- Relevant experience in the pharmaceutical or biotechnology industry, demonstrating the ability to independently manage assigned activities and support broader project goals.
- Working knowledge of multidisciplinary functions involved in product development (e.g., clinical development, biostatistics) and a good understanding of the drug development process.
- Fluency in English, both verbal and written, with strong interpersonal and communication skills.
- Experience in regulatory affairs or related product development functions, and an understanding of clinical trial disclosure and international regulations (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.
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) Specialist 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. As a Regulatory Transparency Specialist, you will be part of a dynamic team dedicated to advancing healthcare solutions, with ample opportunities for professional growth and collaboration in a supportive environment. Our commitment to diversity and flexible working ensures that you can thrive both personally and professionally 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) Specialist
✨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 maybe even a referral.
✨Tip Number 2
Prepare for the interview by understanding Roche's mission and values. Show us how your skills align with their goal of advancing healthcare. Be ready to discuss how you can contribute to their innovative projects.
✨Tip Number 3
Practice common interview questions, but also be prepared for situational ones. Think about how you've handled challenges in past roles, especially in regulatory affairs or project management.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets seen. Plus, it shows you're genuinely interested in joining the Roche team.
We think you need these skills to ace Regulatory Transparency (Disclosures) Specialist
Some tips for your application 🫡
Be Yourself:At StudySmarter, we believe in the power of authenticity. When writing your application, let your unique qualities shine through. Don’t be afraid to show us who you are and what makes you tick!
Tailor Your Application:Make sure to customise your application for the Regulatory Transparency Specialist role. Highlight your relevant experience in regulatory affairs and how it aligns with our mission at Roche. We want to see how you can contribute to our goals!
Show Attention to Detail:As a detail-oriented team player, it’s crucial to demonstrate your organisational skills in your application. Double-check for any typos or inconsistencies, as this reflects your commitment to quality work, which is key in our field.
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 enthusiasm for joining our team!
How to prepare for a job interview at F. Hoffmann-La Roche Gruppe
✨Know Your Stuff
Make sure you brush up on your knowledge of clinical trial disclosure and the regulatory landscape. Familiarise yourself with Roche's values and how they align with your own. This will help you demonstrate your genuine interest in the role and the company.
✨Showcase Your Attention to Detail
As a Regulatory Transparency Specialist, attention to detail is key. Prepare examples from your past experiences where your meticulous nature made a difference. Be ready to discuss how you ensure accuracy in your work, especially under tight deadlines.
✨Emphasise Collaboration Skills
Roche values teamwork, so be prepared to talk about your experience working in cross-functional teams. Share specific instances where you successfully collaborated with others to achieve a common goal, highlighting your communication skills and ability to build relationships.
✨Ask Thoughtful Questions
At the end of the interview, don’t shy away from asking questions. Inquire about the team dynamics, the challenges they face in regulatory disclosures, or how they measure success in this role. This shows your enthusiasm and helps you gauge if the company culture is the right fit for you.