Senior Manager Regulatory Affairs EU Oncology
Senior Manager Regulatory Affairs EU Oncology

Senior Manager Regulatory Affairs EU Oncology

London Full-Time 43200 - 72000 £ / year (est.) No home office possible
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At a Glance

  • Tasks: Lead regulatory strategies for innovative cancer treatments across EU markets.
  • Company: Join a global biotechnology leader dedicated to transforming oncology care.
  • Benefits: Enjoy competitive salary, flexible working options, and comprehensive health benefits.
  • Why this job: Make a real impact in patients' lives while working in a dynamic, collaborative environment.
  • Qualifications: Experience in regulatory affairs, particularly in oncology, is essential.
  • Other info: This role offers the chance to shape the future of cancer treatment.

The predicted salary is between 43200 - 72000 £ per year.

A global biotechnology company is seeking a visionary Regulatory Affairs Senior Manager to drive their expanding oncology portfolio from a strategic perspective. You will play a pivotal role in bringing life-changing cancer treatments from development to patient delivery across EU markets. You will craft regulatory strategies that navigate complex approval pathways and build crucial relationships.

Senior Manager Regulatory Affairs EU Oncology employer: Hays

As a leading global biotechnology company, we pride ourselves on fostering a dynamic and inclusive work culture that empowers our employees to thrive. Located in the heart of the EU, we offer competitive benefits, continuous professional development opportunities, and a collaborative environment where your contributions directly impact the lives of patients. Join us to be part of a mission-driven team dedicated to advancing innovative oncology solutions.
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Contact Detail:

Hays Recruiting Team

StudySmarter Expert Advice 🤫

We think this is how you could land Senior Manager Regulatory Affairs EU Oncology

✨Tip Number 1

Network with professionals in the oncology and regulatory affairs sectors. Attend industry conferences, webinars, or local meetups to connect with key players and gain insights into the latest trends and challenges in the field.

✨Tip Number 2

Stay updated on EU regulations and guidelines related to oncology. Familiarise yourself with recent changes in legislation and how they impact drug approval processes, as this knowledge will be crucial during interviews.

✨Tip Number 3

Prepare to discuss your strategic thinking and problem-solving skills. Be ready to provide examples of how you've successfully navigated complex regulatory pathways in previous roles, showcasing your ability to drive projects forward.

✨Tip Number 4

Research the company’s oncology portfolio and recent developments. Understanding their products and pipeline will allow you to tailor your discussions and demonstrate your genuine interest in contributing to their mission.

We think you need these skills to ace Senior Manager Regulatory Affairs EU Oncology

Regulatory Knowledge in Oncology
Strategic Planning
Project Management
Stakeholder Engagement
Clinical Trial Regulations
EU Regulatory Frameworks
Risk Assessment
Communication Skills
Cross-Functional Collaboration
Problem-Solving Skills
Attention to Detail
Negotiation Skills
Analytical Skills
Adaptability to Change

Some tips for your application 🫡

Understand the Role: Thoroughly read the job description for the Senior Manager Regulatory Affairs EU Oncology position. Understand the key responsibilities and required skills, and think about how your experience aligns with these.

Tailor Your CV: Customise your CV to highlight relevant experience in regulatory affairs, particularly in oncology. Use specific examples that demonstrate your ability to navigate complex approval pathways and develop regulatory strategies.

Craft a Compelling Cover Letter: Write a cover letter that showcases your passion for oncology and regulatory affairs. Explain why you are the ideal candidate for this role and how your vision aligns with the company's mission to deliver life-changing treatments.

Proofread and Edit: Before submitting your application, carefully proofread your CV and cover letter. Check for any spelling or grammatical errors, and ensure that your documents are clear and professional. A polished application reflects your attention to detail.

How to prepare for a job interview at Hays

✨Understand the Regulatory Landscape

Familiarise yourself with the current EU regulatory frameworks, especially those related to oncology. Be prepared to discuss how these regulations impact drug development and approval processes.

✨Showcase Your Strategic Thinking

Highlight your experience in crafting regulatory strategies. Provide examples of how you've successfully navigated complex approval pathways in the past, demonstrating your ability to think critically and strategically.

✨Emphasise Collaboration Skills

Regulatory affairs often require working closely with cross-functional teams. Be ready to share instances where you've collaborated effectively with R&D, clinical, and commercial teams to achieve regulatory goals.

✨Prepare for Scenario-Based Questions

Expect questions that assess your problem-solving skills in real-world scenarios. Think about challenges you've faced in previous roles and how you overcame them, particularly in relation to oncology products.

Senior Manager Regulatory Affairs EU Oncology
Hays
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  • Senior Manager Regulatory Affairs EU Oncology

    London
    Full-Time
    43200 - 72000 £ / year (est.)

    Application deadline: 2027-06-06

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    Hays

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