Head of Research
Listed on 2026-01-22
-
Healthcare
Clinical Research -
Research/Development
Clinical Research, Research Scientist
Contract:
12-month fixed term, full-time (maternity leave cover)
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 RoleWe’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
- 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
- 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
- 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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