At a Glance
- Tasks: Drive global regulatory disclosures and ensure compliance with evolving requirements.
- Company: Join Roche, a leader in medical advancements and ethical commitments.
- Benefits: Flexible working options, competitive salary, and opportunities for professional growth.
- Other info: Collaborative environment with a focus on innovation and transparency.
- Why this job: Make a real impact on patient access to vital clinical information.
- Qualifications: Experience in regulatory affairs and strong project management skills required.
The predicted salary is between 60000 - 80000 € per year.
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.
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.
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.
Regulatory Transparency (Disclosures) Manager in Welwyn employer: Roche
Roche is an exceptional employer that champions transparency and ethical commitments in the healthcare sector, offering a dynamic work culture where innovation thrives. Employees benefit from flexible working arrangements, extensive professional development opportunities, and the chance to make a meaningful impact on global health through their contributions to regulatory transparency. Located in a collaborative environment, team members are encouraged to mentor one another and engage with cross-functional teams, ensuring a fulfilling career path in a leading global organisation.
StudySmarter Expert Advice🤫
We think this is how you could land Regulatory Transparency (Disclosures) Manager in Welwyn
✨Tip Number 1
Network like a pro! Reach out to people in the industry, attend events, and connect on LinkedIn. We all know that sometimes it’s not just what you know, but who you know that can help you land that dream job.
✨Tip Number 2
Prepare for interviews by researching the company and its values. We want you to show how your passion for regulatory transparency aligns with their mission. Practice common interview questions and think about how your experience fits the role.
✨Tip Number 3
Follow up after interviews! A quick thank-you email can go a long way in keeping you top of mind. We suggest mentioning something specific from your conversation to remind them why you’re a great fit.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets seen. Plus, we love seeing candidates who are proactive about their job search.
We think you need these skills to ace Regulatory Transparency (Disclosures) Manager in Welwyn
Some tips for your application 🫡
Show Your Passion for Transparency:Make sure to highlight your enthusiasm for regulatory transparency in your application. We want to see how your values align with our mission at Roche, so share any relevant experiences that demonstrate your commitment to ensuring critical clinical trial data reaches the public.
Tailor Your Application:Don’t just send a generic CV and cover letter! We love it when applicants take the time to tailor their documents to the job description. Mention specific skills and experiences that relate directly to the role of Regulatory Transparency Manager, especially your project management expertise and attention to detail.
Be Clear and Concise:When writing your application, clarity is key. We appreciate well-structured and concise communication, so make sure your points are easy to follow. Use bullet points where appropriate and avoid jargon unless it’s relevant to the role.
Apply Through Our Website:We encourage you to apply through our website for the best chance of being noticed. It’s super easy, and you’ll be able to keep track of your application status. Plus, it shows us you’re genuinely interested in joining our team!
How to prepare for a job interview at Roche
✨Know Your Regulations
Make sure you brush up on global disclosure requirements and regulations relevant to clinical trials. Being able to discuss these confidently will show that you’re not just familiar with the basics, but that you understand the nuances that come with regulatory transparency.
✨Showcase Your Project Management Skills
Prepare examples of how you've successfully managed projects in a cross-functional environment. Highlight your attention to detail and ability to deliver under pressure, as these are crucial for the role. Use the STAR method (Situation, Task, Action, Result) to structure your responses.
✨Demonstrate Collaboration
Think of specific instances where you’ve collaborated with diverse teams. Be ready to discuss how you influenced outcomes and secured buy-in from stakeholders. This will illustrate your ability to work effectively across functions, which is key for this position.
✨Communicate Clearly
Since excellent communication skills are essential, practice articulating your thoughts clearly and concisely. Prepare to explain complex regulatory concepts in simple terms, as you may need to mentor others or present to non-experts during your role.
