Head, AI for Medicines Safety

Head, AI for Medicines Safety

Full-Time 85500 - 104500 £ / year (est.) On-site
The Medicines And Healthcare Products Regulatory Agency

At a Glance

  • Tasks: Lead AI initiatives to enhance medicines safety and improve patient outcomes.
  • Company: Join the MHRA, a leader in regulatory science and innovation.
  • Benefits: Competitive salary, impactful work, and opportunities for professional growth.
  • Other info: Collaborate with top experts across academia, industry, and government.
  • Why this job: Shape the future of healthcare with cutting-edge AI technology.
  • Qualifications: Advanced degree in relevant fields and significant leadership experience required.

The predicted salary is between 85500 - 104500 £ per year.

The MHRA is transforming. Through enabling innovation, making the right judgements of the benefits and risks of medical products and forging the right partnerships in the UK and internationally, it aims to deliver world class regulation and improved outcomes for UK patients. We are currently looking for an experienced Head, AI for Medicines Safety to join our Benefit/Risk Evaluation Team I in the Safety and Surveillance group.

Within a week of working here, your day could look like this:

  • Responsible for the delivery of the MHRA's “Beyond ADMET: AI for Medicines Safety” regulatory sandbox. This strategic regulatory science initiative will explore how artificial intelligence can improve the prediction of absorption, distribution, metabolism, excretion and toxicity (ADMET) outcomes and integrate clinical and real-world data to support safer, faster and more efficient medicines development, ultimately strengthening patient safety.
  • The successful candidate will provide overall leadership for the programme, including its strategic vision, scientific direction and delivery priorities.
  • The role requires a leader who can operate at the intersection of regulatory science, artificial intelligence, medicines development and patient safety, bringing together expertise from across the MHRA, academia, industry, government and the wider healthcare ecosystem.
  • The Head, AI for Medicine Safety will be accountable for ensuring that programme activities are scientifically and technically robust, and aligned with the MHRA strategic objectives.
  • The postholder will act as the senior ambassador for the programme, building partnerships nationally and internationally, influencing emerging regulatory thinking, and helping position the MHRA as a global leader in AI-enabled regulation and patient safety science.
  • Initially focused on leading delivery of the “Beyond ADMET: AI for Medicines Safety” regulatory sandbox programme, the postholder will also contribute to the MHRA's broader strategic ambitions in AI-enabled regulatory science and innovation, with opportunities to apply their expertise across other priority areas as organisational needs evolve.

The successful candidate will have a degree in a relevant scientific, technical or healthcare discipline (or equivalent experience). Postgraduate qualification (MSc, PhD or equivalent experience) in a relevant field such as artificial intelligence, computational biology, pharmacology, toxicology, data science, bioinformatics, pharmaceutical sciences or a related discipline.

Recognised expertise in either:

  • Artificial Intelligence, Machine Learning, Data Science or Computational Modelling; or
  • Pharmacology, Toxicology, Drug Development, NAMs or related life science disciplines.

Broad understanding of the wider AI and medicines development ecosystem, with the ability to lead multidisciplinary teams spanning both domains. Ability to evaluate scientific evidence and emerging technologies and translate findings into regulatory and strategic recommendations.

Our successful candidate will have:

  • Significant senior leadership experience in one or more relevant disciplines, including:
    • Artificial Intelligence and Machine Learning
    • Computational modelling
    • Pre-clinical assessment, toxicology and New Approach Methodologies (NAMs)
    • Pharmacology, drug discovery or development
    • Healthcare data science or related scientific areas.
  • Experience leading complex strategic programmes, scientific portfolios or major innovation initiatives, and successful delivery of their outcomes.
  • Experience managing multidisciplinary teams and leading highly specialised technical experts.
  • Experience influencing senior stakeholders, operating effectively across organisational boundaries and working collaboratively with external partners including academia, industry, government and healthcare organisations.

Head, AI for Medicines Safety employer: The Medicines And Healthcare Products Regulatory Agency

The MHRA is an exceptional employer, offering a dynamic work environment where innovation and collaboration thrive. As part of the Clinical Practice Research Datalink team, you will have the opportunity to enhance your Azure expertise while contributing to vital health research that impacts patient outcomes across the UK. With a strong focus on employee development and a commitment to operational excellence, the MHRA fosters a culture of continuous improvement and meaningful engagement in the healthcare sector.

The Medicines And Healthcare Products Regulatory Agency

Contact Details:

The Medicines And Healthcare Products Regulatory Agency Recruitment Team

StudySmarter Expert Advice🤫

We think this is how you could land Head, AI for Medicines Safety

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✨Stay Updated with Industry Trends

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We think you need these skills to ace Head, AI for Medicines Safety

Artificial Intelligence
Machine Learning
Data Science
Computational Modelling
Pharmacology
Toxicology
Drug Development

Some tips for your application 🫡

Highlight Your Relevant Experience:When applying for a role in health sciences administration, it's super important to spotlight any relevant experience you have in healthcare settings. Whether you've worked in a hospital, a clinic, or any related environment, make sure to detail those roles in your CV – focusing on your responsibilities and achievements that align with the job at The Medicines And Healthcare Products Regulatory Agency.

Showcase Your Administrative Skills:Administrative skills are key in this field, so don’t hold back! Make sure your CV reflects your proficiency in things like scheduling, data management, and compliance with health regulations. Mention specific software you’ve used, such as patient management systems, as this will demonstrate your hands-on abilities and readiness for the role at The Medicines And Healthcare Products Regulatory Agency.

Craft a Meaningful Cover Letter:Your cover letter should reflect your passion for the health sciences field and your eagerness to contribute to The Medicines And Healthcare Products Regulatory Agency. Share a bit about why you’re drawn to this sector, any impactful situations or challenges you’ve encountered, and how they’ve shaped your desire to work in health sciences administration. This personal touch can really set you apart!

Tailor Your Documents to the Job:Don't use a one-size-fits-all approach! Make sure your CV and cover letter are specifically tailored for this role. Highlight any certifications you have relevant to health administration, and ensure you clearly connect your previous roles to the skills needed for the full-time position at The Medicines And Healthcare Products Regulatory Agency. This way, you're showing them you’ve done your homework and are genuinely interested in being a part of their team.

How to prepare for a job interview at The Medicines And Healthcare Products Regulatory Agency

✨Showcase Your Administrative Skills

In health sciences administration, being organised is key. Make sure you can demonstrate your skills in managing schedules, paperwork, and data accurately. Be ready to discuss specific tools you've used, like electronic health record systems or scheduling software, and how they improved efficiency in your past experiences.

✨Know Your Regulations

Familiarity with healthcare regulations and compliance is crucial. Brush up on HIPAA, GDPR, or other relevant policies before your interview. We recommend preparing examples of how you've ensured compliance or handled sensitive information in past roles—this will show you're not just knowledgeable but also responsible.

✨Prepare for Scenario Questions

Interviews for administrative roles often involve scenario-based questions to assess your problem-solving skills. Practice responses to common situations you might face, such as dealing with a challenging patient or managing a sudden schedule change. This will not only demonstrate your ability to think on your feet but also highlight your interpersonal skills.

✨Align Your Goals with the Organisation

As a full-time candidate, employers will want to know how your long-term career goals align with their mission. Take some time to research The Medicines And Healthcare Products Regulatory Agency’s values and be ready to tie your passion for health sciences administration into their objectives. Demonstrating enthusiasm and career alignment can be a game-changer in this competitive field!