Regulatory Program Manager

Regulatory Program Manager

London Full-Time 36000 - 60000 £ / year (est.) No home office possible
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At a Glance

  • Tasks: Manage regulatory information and ensure smooth submission processes.
  • Company: Roche is a global leader in healthcare, dedicated to innovation and patient care.
  • Benefits: Enjoy a supportive culture, opportunities for personal growth, and impactful work.
  • Why this job: Join a diverse team making a real difference in global healthcare.
  • Qualifications: Bachelor's degree in biology, chemistry, English, or related field required.
  • Other info: Experience with Veeva Vault RIM is a plus; embrace your unique self at Roche.

The predicted salary is between 36000 - 60000 £ 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 Opportunity: Are you ready to innovate, collaborate, and create impactful outcomes? Join us as a Regulatory Program Manager in the Pharma Technical Regulatory Submission Management Group. In this role, you will play a pivotal part in global planning, tracking, and monitoring of regulatory information crucial for compliance and successful submission execution.

  • Manage regulatory information activities in coordination with the regulatory product portfolio team.
  • Partner with various departments to ensure seamless submission processes.
  • Oversee the formatting (and editing) of technical documents.
  • Coordinate document flow within the management system and ensure version control throughout the submission process.
  • Ensure timely delivery of content and maintain clear communication with technical subject-matter experts.

Who You Are: A graduate with a Bachelor's or higher degree in biology, chemistry, English, or a related field. Proficient in document management best practices and comfortable with diverse digital tools. Skilled at building productive relationships across departments and with external partners, thriving in a diverse team. An effective problem-solver with excellent interpersonal skills, able to prioritize multiple tasks. Committed to continuous improvement, always looking for ways to enhance processes, systems, and tools, and open to giving and receiving feedback. Experience with Veeva Vault RIM is desirable.

Join us and be part of a team dedicated to making a difference for patients, stakeholders, and our company. Apply now and help us drive innovation in regulatory submissions!

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.

Regulatory Program Manager employer: F. Hoffmann-La Roche Gruppe

At Roche, we pride ourselves on being an exceptional employer, fostering a culture of inclusivity and personal expression that allows our employees to thrive. As a Regulatory Program Manager, you will benefit from a collaborative work environment that values your unique contributions, alongside opportunities for professional growth and development. Located in a dynamic setting, you will be part of a team dedicated to making a meaningful impact in healthcare, ensuring that every voice is heard and valued.
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Contact Detail:

F. Hoffmann-La Roche Gruppe Recruiting Team

StudySmarter Expert Advice 🤫

We think this is how you could land Regulatory Program Manager

✨Tip Number 1

Familiarise yourself with the regulatory landscape in the pharmaceutical industry. Understanding the key regulations and compliance requirements will not only help you in interviews but also demonstrate your commitment to the role.

✨Tip Number 2

Network with professionals in the regulatory field, especially those who have experience with Veeva Vault RIM. Engaging in conversations can provide insights into the role and may even lead to referrals.

✨Tip Number 3

Prepare to discuss specific examples of how you've managed document flows or improved processes in previous roles. This will showcase your problem-solving skills and ability to enhance systems, which are crucial for this position.

✨Tip Number 4

Demonstrate your interpersonal skills by being ready to talk about how you've built relationships across departments. Highlighting your collaborative experiences will align well with Roche's emphasis on teamwork and communication.

We think you need these skills to ace Regulatory Program Manager

Regulatory Knowledge
Document Management Best Practices
Technical Writing and Editing
Project Management
Interpersonal Skills
Problem-Solving Skills
Attention to Detail
Version Control
Communication Skills
Collaboration Skills
Time Management
Continuous Improvement Mindset
Familiarity with Veeva Vault RIM
Ability to Prioritise Tasks

Some tips for your application 🫡

Understand the Role: Before applying, make sure you fully understand the responsibilities of a Regulatory Program Manager at Roche. Highlight your relevant experience in regulatory information management and document handling in your application.

Tailor Your CV: Customise your CV to reflect the skills and qualifications mentioned in the job description. Emphasise your proficiency in document management practices and any experience with tools like Veeva Vault RIM.

Craft a Compelling Cover Letter: Write a cover letter that showcases your passion for healthcare and innovation. Mention how your background in biology, chemistry, or English aligns with Roche's mission and values, and express your commitment to continuous improvement.

Proofread Your Application: Before submitting, carefully proofread your application materials. Ensure there are no spelling or grammatical errors, and that your documents are well-formatted and professional. This reflects your attention to detail, which is crucial for the role.

How to prepare for a job interview at F. Hoffmann-La Roche Gruppe

✨Understand the Role

Make sure you thoroughly understand the responsibilities of a Regulatory Program Manager. Familiarise yourself with regulatory submission processes and document management best practices, as these will likely be key discussion points during your interview.

✨Showcase Your Interpersonal Skills

Since the role involves collaborating with various departments, be prepared to discuss examples of how you've built productive relationships in previous roles. Highlight your ability to communicate effectively and work within diverse teams.

✨Demonstrate Problem-Solving Abilities

Prepare to share specific instances where you've successfully solved problems or improved processes. This will showcase your commitment to continuous improvement, which is highly valued in this position.

✨Familiarise Yourself with Veeva Vault RIM

If you have experience with Veeva Vault RIM, be ready to discuss it. If not, do some research on it beforehand. Showing that you're proactive about learning new tools can set you apart from other candidates.

Regulatory Program Manager
F. Hoffmann-La Roche Gruppe
F
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