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Head of Research

Job in Greater London, London, Greater London, W1B, England, UK
Listing for: myota
Full Time, Contract position
Listed on 2026-01-22
Job specializations:
  • Healthcare
    Clinical Research
  • Research/Development
    Clinical Research, Research Scientist
Job Description & How to Apply Below
Location: Greater London

Contract:

12-month fixed term, full-time (maternity leave cover)

About us

At myota, we’re transforming gut health with cutting-edge science and clinically proven innovation. Founded by world-leading microbiome scientists and seasoned operators, and backed by Europe’s top VCs, myota is pioneering a new era of prebiotic fibre products - clinically effective, patented, and built on groundbreaking research from MIT.

With over 50,000 customers and strong adoption among doctors, dietitians and nutritionists, we’re already making a meaningful difference. Our clinical research programme spans partnerships with the NHS and leading universities, placing us at the forefront of evidence-based gut health.

You’ll be joining us at a pivotal moment in our growth - a small, high-impact team on a mission to prevent and reverse the 1 billion cases of chronic disease linked to poor gut health. We’re here to extend healthy lifespans, one gut at a time.

About the Role

We’re looking for a Head of Research to cover a 12-month maternity leave. This role is central to delivering our research strategy, overseeing clinical trial operations, and supporting our B2B/D2C/HCP science communications. The ideal candidate will bring strong expertise in clinical trials, nutrition, and the gut microbiome, alongside excellent organisational and scientific communication skills.

Key Responsibilities Clinical Trial Operations
  • Setting up, managing, and monitoring large-scale human clinical trials
  • Developing, editing, and reviewing study protocols, participant materials (PIC/ICF), and supporting documentation with appropriate document provenance
  • Developing statistical analysis plans
  • Managing trial governance, including ethics submissions and amendments, GCP compliance, regulatory approvals, insurance, reporting, and sponsor oversight
  • Overseeing participant consent, enrolment processes, safety monitoring, ongoing risk assessment, and (S)
    AE management
  • Ensuring high-quality data collection on EDC platforms, including auditing and QC processes
  • Coordinating sample collection procedures, including compliance with the Human Tissue Act and correct handling and storage of biological samples (including gut microbiome sample handling and analysis)
  • Liaising with external laboratories, contractors, and CROs to support analysis and sample processing
  • Responsible for ensuring recruitment targets are met, and initiating mitigation strategies to ensure trial deadlines remain on track
  • Acting as Lead Study Sponsor, working closely with PIs and clinical trial centres
  • Managing large study budgets and monthly reporting
  • Familiarity with EFSA/FDA health claims
Research & Development (R&D)
  • Lead and contribute to research protocols, scientific reports, and peer-reviewed publications
  • Generate research ideas aligned with myota’s scientific and commercial goals
  • Manage CRO-led studies and monitor milestones such as participant recruitment and endpoint delivery
  • Design and implement study endpoints involving clinical outcomes, questionnaires, or biomarker analysis
  • Write or update internal SOPs and research documentation
  • Finding new opportunities for grants/funding opportunities and writing/submitting applications
  • Presenting at scientific events and conferences, and building academic, industry and NHS partnerships
Scientific Communication
  • Communicate myota’s research, clinical evidence, and scientific positioning clearly to prospective B2B clients and partners
  • Delivering external talks to a range of audiences/stakeholders
  • Creating scientific resources, and producing research graphics or summaries
  • Develop educational resources for consumers and HCPs
  • Review or contribute to newsletters, email journeys, blogs, and social content
  • Provide regulatory oversight on health claims and advertising copy
Experience/Qualifications
  • PhD or Master’s degree in nutrition, gut microbiome, biomedical sciences, or a related field
  • Registered dietitian or Association for Nutrition (AfN) Registered Nutritionist
  • Experience in microbiome science, clinical nutrition, or functional food product development
  • Demonstrated experience managing human clinical trials is a must
  • Strong written and verbal communication skills, with the…
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