At a Glance
- Tasks: Lead the design and execution of clinical validation studies for innovative diagnostic assays.
- Company: Join Pictura Bio, a cutting-edge spin-out from the University of Oxford.
- Benefits: Full-time role with opportunities for professional growth in a dynamic environment.
- Why this job: Make a real impact in rapid pathogen detection and improve healthcare outcomes.
- Qualifications: PhD, MD, or MSc in relevant fields with experience in validating diagnostic assays.
- Other info: Collaborate with top professionals in a fast-paced, scaling diagnostics company.
The predicted salary is between 60000 - 80000 £ per year.
Pictura Bio is a well‑funded University of Oxford spin‑out developing a novel diagnostic platform for rapid pathogen detection. Our technology combines fluorescence microscopy with automated image analysis and machine learning to identify pathogens in seconds. The platform is being translated into clinical diagnostic products, initially focused on respiratory infections, with broader applications across infectious disease.
The Clinical Validation Lead will be responsible for designing, executing, and overseeing clinical and analytical validation of Pictura Bio’s diagnostic assays. You will lead validation strategy from late‑stage development through clinical evaluation, ensuring studies are scientifically robust, regulator‑ready, and aligned with the intended clinical use. This role is ideal for someone with hands‑on experience validating diagnostic assays in regulated environments, particularly US LDTs, but experience with FDA‑cleared/approved, UK, or EU IVD pathways is also highly relevant. You will work closely with assay development, data science, regulatory, and external clinical partners.
Major Accountabilities
- Lead the design and execution of analytical and clinical validation studies for diagnostic assays
- Define validation plans covering precision, accuracy, sensitivity/specificity, LoD, reproducibility, interference, and cross‑reactivity
- Ensure validation studies are aligned with intended use, clinical claims, and regulatory expectations
- Oversee clinical sample selection, handling, and testing in collaboration with partner laboratories and CROs
- Support validation of Laboratory Developed Tests (LDTs), particularly within the US regulatory framework
- Contribute to validation supporting FDA (e.g. De Novo / 510(k)), UKCA, or CE‑IVD pathways where applicable
- Review and approve protocols, reports, and data summaries for internal and external use
- Work with data science teams to ensure clinical performance metrics and analyses are appropriate and traceable
- Interface with regulatory and quality teams to support technical files, submissions, and audits
- Manage external stakeholders (clinical sites, reference labs, CROs) involved in validation activities
- Clearly communicate validation strategy, results, and risks to senior leadership
Ideal Background
Education
- PhD, MD, PharmD, or MSc in a relevant discipline (e.g. Clinical Sciences, Biomedical Sciences, Molecular Biology, Immunology, Microbiology)
Experience
- Demonstrated experience clinically validating diagnostic assays
- Experience with assays such as immunofluorescence, molecular diagnostics, NGS / optical sequencing (e.g. Illumina), or imaging‑based diagnostics
- Experience developing or validating US Laboratory Developed Tests (LDTs) is highly desirable
- Experience supporting FDA‑cleared/approved assays (De Novo, 510(k), PMA) or UK/EU IVD pathways is advantageous
- Experience working with clinical samples (e.g. respiratory samples, blood, urine, swabs)
- Experience collaborating with hospital labs, reference labs, or CROs
Skills
- Deep understanding of diagnostic validation principles and study design
- Strong knowledge of clinical performance metrics and statistical interpretation
- Familiarity with regulatory and quality frameworks (e.g. CLIA, CAP, ISO 13485, ISO 15189)
- Ability to translate clinical requirements into practical validation studies
- Strong documentation, reporting, and review skills
- Excellent communication skills, including interaction with clinicians, regulators, and executives
- Highly organised and detail‑oriented, with a strong quality mindset
- Comfortable taking ownership of complex, multi‑stakeholder validation programmes
- Scientifically rigorous but pragmatic in balancing timelines and regulatory expectations
- Confident communicator who can explain validation decisions clearly
- Comfortable working in a fast‑moving, scaling diagnostics company
Seniority level Mid‑Senior level
Employment type Full‑time
Job function Health Care Provider
Industries Hospitals and Health Care
Clinical Validation Lead – Diagnostics Assay in England employer: PicturaBio
Contact Detail:
PicturaBio Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Clinical Validation Lead – Diagnostics Assay in England
✨Tip Number 1
Network like a pro! Reach out to professionals in the diagnostics field, especially those who have experience with clinical validation. Attend industry events or webinars to make connections and learn more about the latest trends.
✨Tip Number 2
Prepare for interviews by brushing up on your knowledge of regulatory frameworks and validation principles. Be ready to discuss your hands-on experience with diagnostic assays and how you've tackled challenges in previous roles.
✨Tip Number 3
Showcase your communication skills! During interviews, clearly articulate your validation strategies and how you’ve collaborated with cross-functional teams. This will demonstrate your ability to lead and manage complex projects.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets noticed. Plus, it shows your enthusiasm for joining Pictura Bio and being part of our innovative team.
We think you need these skills to ace Clinical Validation Lead – Diagnostics Assay in England
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the Clinical Validation Lead role. Highlight your relevant experience in validating diagnostic assays and any specific regulatory pathways you've worked with. We want to see how your background aligns with what we're looking for!
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you're passionate about diagnostics and how your skills can contribute to our mission at Pictura Bio. Be sure to mention any hands-on experience you have with clinical validation.
Showcase Your Communication Skills: Since this role involves interfacing with various stakeholders, it's crucial to demonstrate your communication skills. In your application, give examples of how you've effectively communicated complex validation strategies or results to different audiences.
Apply Through Our Website: We encourage you to apply directly through our website. It’s the best way for us to receive your application and ensures you’re considered for the role. Plus, it shows your enthusiasm for joining our team at Pictura Bio!
How to prepare for a job interview at PicturaBio
✨Know Your Stuff
Make sure you brush up on the latest trends in diagnostic validation, especially around LDTs and regulatory pathways like FDA and UKCA. Being able to discuss specific examples from your experience will show that you're not just familiar with the theory but have practical knowledge too.
✨Prepare for Technical Questions
Expect to dive deep into technical aspects of assay validation. Be ready to explain concepts like sensitivity, specificity, and reproducibility. Practising how to articulate these terms clearly will help you communicate effectively with both technical and non-technical interviewers.
✨Showcase Your Collaboration Skills
Since this role involves working closely with various teams, be prepared to share examples of how you've successfully collaborated with clinical partners or CROs in the past. Highlighting your ability to manage relationships and communicate clearly will set you apart.
✨Ask Insightful Questions
At the end of the interview, don’t shy away from asking questions about Pictura Bio’s current projects or future directions. This shows your genuine interest in the company and helps you gauge if it’s the right fit for you. Plus, it gives you a chance to demonstrate your knowledge about their technology!