Associate Director, Regulatory Affairs - UK & Ireland

Associate Director, Regulatory Affairs - UK & Ireland

Full-Time 80700 - 100900 £ / year (est.) Working from home possible
BeiGene

At a Glance

  • Tasks: Lead regulatory strategies for cancer-fighting products in the UK and Ireland.
  • Company: BeOne, a rapidly growing biotech company dedicated to fighting cancer.
  • Benefits: Competitive salary, remote work, and opportunities for professional growth.
  • Other info: Join a collaborative team focused on innovation and excellence.
  • Why this job: Make a real impact in the fight against cancer while advancing your career.
  • Qualifications: 8+ years in regulatory affairs, with experience in oncology and MHRA procedures.

The predicted salary is between 80700 - 100900 £ per year.

BeOne continues to grow at a rapid pace with challenging and exciting opportunities for experienced professionals. When considering candidates, we look for scientific and business professionals who are highly motivated, collaborative, and most importantly, share our passionate interest in fighting cancer.

General Description: The Associate Director of Regulatory Affairs will be responsible for developing and implementing UK regulatory strategies for development programs to secure and maintain the marketing authorization for product(s) in line with business objectives, and in coordination with key internal stakeholders. This will also include oversight and management of commercial products for both UK and Ireland.

Essential Functions of the job:

  • This individual will lead the UK RA team to manage regulatory aspects of designated compounds (NME/New indications) through all phases of development, registration, post-approval, and lifecycle of the product.
  • Collaborate with key internal stakeholders to define UK MAA strategy and ensure the regulatory strategy is incorporated and implemented in line with product development objectives.
  • Manage the content of and prepare regulatory (UK MAA) dossiers. Have knowledge of the content of the EU MAA dossiers to support labeling updates and management in Ireland ensuring compliance with UK and Ireland regulatory requirements.
  • Oversee and be accountable for regulatory agency communications, submissions, and approvals, with a quality focus to secure first-cycle/attempt approvals.
  • Review and provide input into promotional materials for both UK and Ireland.
  • Act as the RA liaison within the UK Leadership team, attend regular meetings and provide input into UK business strategy.
  • Prepare team for HA interactions, and moderate and lead discussions, be the main MHRA contact for strategic, non-study specific topics and provide support to the EU RA team for clinical matters related to Health Authority topics.
  • Proactively anticipate and mitigate regulatory risks while maintaining current knowledge of regulatory intelligence, procedures, changes, and trends.
  • Provide submission gap analyses, identify potential risks and propose potential solutions/mitigation plans to ensure successful acceptance of submissions.
  • Ensure compliance with EU/UK global regulatory requirements.
  • Lead and mentor junior team members.
  • Represent BeOne at UK industrial association meetings and congresses.

Supervisory Responsibilities: Junior Regulatory Affairs professionals.

Computer Skills: Extensive experience with Microsoft Office suite, Veeva regulatory publishing and expertise with PowerPoint presentation authoring and presentation.

Education Required: Bachelor’s degree required; advanced degree preferred.

Other Qualifications: Minimum of 8 years’ experience in the biotechnical or pharmaceutical industry, and a minimum of 8 years’ experience in a Regulatory capacity with a broad background. Experience working with MHRA regulatory procedures is mandatory for this role. Sound understanding of the drug development process, the pharmaceutical industry and healthcare environment including UK regulatory requirements and policy trends. Recent experience with oncology products and MAAs, ODD, PIP is preferred. Proven ability to deliver on goals within a cross-functional team/partnership environment with a high level of professionalism.

Location: UK, fully remote.

Travel: Travel to internal meetings in UK monthly or bimonthly. Additional travel to EU locations occasionally.

Salary Range UK: 80,700.00 GBP - 100,900.00 GBP.

Global Competencies: When we exhibit our values of Patients First, Driving Excellence, Bold Ingenuity, and Collaborative Spirit, through our twelve global competencies below, we help get more affordable medicines to more patients around the world.

  • Fosters Teamwork
  • Provides and Solicits Honest and Actionable Feedback
  • Self-Awareness
  • Acts Inclusively
  • Demonstrates Initiative
  • Entrepreneurial Mindset
  • Continuous Learning
  • Embraces Change
  • Results-Oriented
  • Analytical Thinking/Data Analysis
  • Financial Excellence
  • Communicates with Clarity

We are proud to be an equal opportunity employer. BeOne does not discriminate on the basis of race, religion, color, sex, gender identity, sexual orientation, age, disability, national origin, veteran status or any other basis covered by appropriate law. All employment is decided on the basis of qualifications, merit, and business need.

Associate Director, Regulatory Affairs - UK & Ireland employer: BeiGene

BeOne is an exceptional employer that fosters a collaborative and innovative work culture, dedicated to fighting cancer through rigorous clinical compliance. Employees benefit from a supportive environment that prioritises professional growth, offering opportunities for continuous learning and development in a fast-paced, multicultural setting. With a commitment to patient safety and data integrity, BeOne ensures that its team members are empowered to make a meaningful impact in the healthcare sector.

BeiGene

Contact Details:

BeiGene Recruitment Team

StudySmarter Expert Advice🤫

We think this is how you could land Associate Director, Regulatory Affairs - UK & Ireland

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We think you need these skills to ace Associate Director, Regulatory Affairs - UK & Ireland

Regulatory Affairs
UK MAA Strategy Development
EU MAA Dossier Knowledge
Regulatory Agency Communication
Submission Management
Risk Mitigation
Regulatory Compliance

Some tips for your application 🫡

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How to prepare for a job interview at BeiGene

Understand the Science

Make sure you brush up on key pharmaceutical concepts and recent developments in the industry. You might get asked some technical questions during the interview at BeiGene that show your grasp of drug development processes or regulatory requirements, so be ready to discuss them clearly.

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If you have any hands-on experience or internships in a laboratory setting, be sure to highlight these in your responses. Think about the projects you worked on, the methodologies you used, and the impact you made. It's all about telling a story that connects your background to the role you're applying for.

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