At a Glance
- Tasks: Transform regulatory intelligence into actionable insights to accelerate medicine delivery.
- Company: Join AstraZeneca, a leader in inclusive healthcare innovation.
- Benefits: Competitive salary, collaborative culture, and opportunities for professional growth.
- Other info: Dynamic environment with diverse teams and a focus on continuous learning.
- Why this job: Make a real impact on patient outcomes through strategic regulatory insights.
- Qualifications: Advanced degree in science and strong analytical skills required.
The predicted salary is between 80000 - 100000 £ per year.
This job is with AstraZeneca, an inclusive employer and a member of myGwork – the largest global platform for the LGBTQ+ business community.
Location: Cambridge
Salary: competitive
Introduction to role:
Are you ready to turn regulatory intelligence into decisive advantage that accelerates medicines to patients? This role sits at the intersection of competitive insight, regulatory science, and portfolio strategy translating emerging signals into clear regulatory choices for our pipeline and marketed assets.
You will partner closely with senior regulatory leaders and cross-functional intelligence groups to anticipate shifts in guidance, identify precedent that unlocks smarter development pathways, and shape responses that influence external policy. In an agile, collaborative environment, you will help convert complex data into action that shortens timelines, strengthens labels, and improves patient outcomes.
Accountabilities:
- Conduct analysis and impact assessment of Regulatory Intelligence across the portfolio in a given therapeutic area (TA) and communicate findings to key stakeholders and senior leaders within the assigned therapeutic area.
- Work closely with other Intelligence groups within the company (PIRS, GIACE, Clinical Information Science, etc) to provide the disease area/scientific platform specific Regulatory interpretation and impact.
- Serve as the central point person within TA in leading bespoke Regulatory research for RADs including project level Regulatory strategy, due diligence, disease area strategy, initiatives etc.
- Partner with International, China, and Japan Regulatory Affairs Directors to align on TA-specific guidance and regulatory intelligence across regions; contribute to the holistic regulatory landscape by disease/scientific platform and coordinate with PIRS to gather input and provide feedback on draft guidance and policies.
- Proactively conduct analysis of new drug development and regulatory approaches on e.g. novel clinical trial concepts, RWE, early regulatory access, adaptive/conditional licensing as it relates to the TA.
- Research and analyze Regulatory guidance, precedence, and other asset-specific research projects to support our products and development pipeline per market/region.
- Review relevant regulatory assessment documents from agencies to extract key insights in supporting Regulatory landscaping and strategy.
- Perform research and analysis of relevant Regulatory hearings providing pre-meeting briefings and post-meeting impact analysis to key stakeholders and senior leaders within the Company.
- In coordination with functions in the TA, liaise with Reg Ex/PIRS to support their development and deployment of new technologies, including artificial intelligence, to facilitate regulatory intelligence.
Essential Skills/Experience:
- An advanced degree in a science related field and/or other appropriate knowledge/experience.
- Demonstrate competencies of strategic thinking, data and impact analysis, and excellent oral and written communication skills.
- In-depth knowledge of the designated therapeutic area.
- Ability to evaluate the impact of key Regulatory Intelligence on disease area and project strategy.
- Ability to critically distinguish between "noise" and meaningful news to key stakeholders and senior leaders.
- Have a working knowledge about Regulatory Intelligence tools and stay current with regulatory news regarding key competitors and the disease area.
- Have a solid knowledge of US and European Regulatory Affairs.
- Have a good understanding of drug development.
Desirable Skills/Experience:
- A good understanding of the commercial aspects of drug development.
- Broad background of experience working in the pharmaceutical business and prior experience in several areas within regulatory affairs; experience in the relevant therapy area (small molecules and biologics) is preferred.
- Critical thinking on current global regulatory science trends and questions, with a good understanding of the corresponding scientific and clinical components.
Why AstraZeneca:
Here, regulatory intelligence directly shapes strategy from the earliest stages through approval and beyond-bringing life-changing medicines to patients faster. You will work in a fast-moving, collaborative setting where diverse experts come together to challenge assumptions, influence external regulators on new technologies, and design progressive solutions. Expect unexpected teams in the same room unleashing bold thinking, backed by leaders who remove barriers and value kindness alongside ambition. With a strong focus on analytics, technology adoption, and continuous learning, you will broaden your impact across modalities and stages of development while honing your craft through clear development paths and a culture that shares, tests, and improves ideas together.
What is next:
Ready to make a positive impact? Apply now to join our journey towards operational excellence!
So, what's next? Complete your application before the below closing date 9th June 2026.
Where can I find out more? Follow AstraZeneca on LinkedIn, Facebook, and Instagram.
Salary: Negotiable
Regulatory Affairs Intelligence Director employer: AstraZeneca
AstraZeneca is an exceptional employer that fosters an inclusive and collaborative work culture, where regulatory intelligence plays a pivotal role in shaping strategies that accelerate the delivery of life-changing medicines to patients. Located in Cambridge, employees benefit from a dynamic environment that encourages continuous learning, innovative thinking, and professional growth, supported by leaders who prioritise kindness and ambition. With a strong emphasis on analytics and technology adoption, AstraZeneca offers clear development paths and opportunities to make a meaningful impact in the pharmaceutical industry.
StudySmarter Expert Advice🤫
We think this is how you could land Regulatory Affairs Intelligence Director
✨Tip Number 1
Network like a pro! Reach out to folks in the industry, especially those at AstraZeneca. Use LinkedIn to connect and engage with them. A friendly chat can sometimes open doors that applications can't.
✨Tip Number 2
Prepare for interviews by diving deep into AstraZeneca's recent projects and regulatory strategies. Show them you’re not just another candidate; you’re someone who’s genuinely interested in their mission and ready to contribute.
✨Tip Number 3
Practice your pitch! Be ready to explain how your skills align with the role of Regulatory Affairs Intelligence Director. Highlight your strategic thinking and data analysis abilities – they want to see you can turn insights into action.
✨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 serious about joining the team at AstraZeneca.
We think you need these skills to ace Regulatory Affairs Intelligence Director
Some tips for your application 🫡
Tailor Your Application:Make sure to customise your CV and cover letter for the Regulatory Affairs Intelligence Director role. Highlight your relevant experience and skills that align with the job description, especially in regulatory intelligence and strategic thinking.
Showcase Your Analytical Skills:Since this role involves a lot of data analysis and impact assessment, be sure to include examples of how you've successfully conducted similar analyses in the past. We want to see your ability to turn complex data into actionable insights!
Communicate Clearly:Your written communication skills are crucial for this position. Keep your application clear and concise, avoiding jargon unless necessary. We appreciate straightforward language that gets your point across effectively.
Apply Through Our Website:Don’t forget to submit your application through our official website! It’s the best way for us to receive your details and ensure you’re considered for the role. Plus, it shows you’re serious about joining our team!
How to prepare for a job interview at AstraZeneca
✨Know Your Regulatory Stuff
Make sure you brush up on the latest regulatory news and trends, especially in the therapeutic area you're applying for. Familiarise yourself with AstraZeneca's pipeline and how regulatory intelligence plays a role in their strategy.
✨Showcase Your Analytical Skills
Prepare to discuss specific examples where you've conducted impact assessments or analyses in your previous roles. Be ready to explain how your insights influenced decision-making and improved outcomes.
✨Communicate Clearly
Since this role involves liaising with senior leaders and cross-functional teams, practice articulating complex ideas simply and effectively. Use clear examples to demonstrate your communication skills during the interview.
✨Be Collaborative
AstraZeneca values teamwork, so think of instances where you've successfully collaborated with others. Highlight your ability to work across different functions and regions, and how that has led to successful regulatory strategies.
