Senior Research Scientist - Clinical and Regulatory Expertise

Flo Health Inc.; Greater London; Hybrid; GBP 80,000 - 100,000; Part time

Job summary

A leading health-tech company in London is seeking a Senior Research Scientist to oversee clinical studies and contribute to regulatory document preparation. This position requires expertise in data analysis, clinical research, and the ability to produce scientific publications. Ideal candidates will have a PhD in Public Health or a related field, along with proficiency in statistical analysis software like Python and R. Competitive salary, flexible work arrangements, and comprehensive benefits are offered.

Benefits

Competitive salary

Paid holiday and sick leave

Enhanced parental leave

5-week sabbatical after 5 years

Flexible working arrangements

Qualifications

• PhD or Postdoc in Public Health, Biostatistics, or related fields.
• Experience leading design and execution of clinical research studies.
• Familiarity with FDA, EU MDR compliance.
• Strong data analysis skills in Python and R.

Responsibilities

• Provide scientific input and oversight for clinical studies.
• Assemble regulatory documents for FDA submission.
• Analyze large datasets and perform statistical analysis.
• Write and publish research papers in peer-reviewed journals.

Skills

Data analysis

Clinical research

Statistical analysis

Publication writing

Education

PhD or Postdoc in relevant fields

Tools

Python

R

SQL

Job description

Senior Research Scientist - Clinical and Regulatory Expertise (contract)

London

Flo is the world’s #1 health & fitness app worldwide on a mission to build a better future for female health. Backed by a $200M investment led by General Atlantic, we became the first product of our kind to reach a $1B valuation in 2024 – and we’re not slowing down.

With 6M paid subscribers and the highest-rated experience in the App Store’s health category, we’ve spent 10 years earning trust at scale. Now, we’re building the next generation of digital health – AI-powered, privacy-first, clinically backed – to help our users know their body better.

The Role

The Role: Setting the gold standard for software as a medical device

We are seeking a highly skilled Senior Research Scientist to join our Science team for 20-30 hours per week. This role is centered on working with big data to answer research questions within Women’s Health to write a first-author paper for a top-tier journal. You will also be supporting the successful execution of our clinical investigation into the safety and effectiveness of our new medical device, and the scientific strategy and planning for future devices. The mission of your job is to bridge the gap between "interesting research", "clinical proof", “regulatory requirements”, and “business metrics”.

You will work closely with the Lead Research Scientist and the Director of Science, but your impact of research will be felt through the whole company, across the legal, compliance, and product teams.

What you\'ll be doing

• Provide day-to-day scientific input and oversight for ongoing clinical studies. This involves data analysis, manuscript writing, and ensuring protocol adherence across teams.
• Assemble high-quality regulatory documents (including study protocols, statistical analysis plans, study reports) for submission to the FDA and notified bodies (EU MDR).
• Prepare, extract, and analyze large-scale datasets, performing statistical analysis and developing reporting specifications (SAPs, sample size estimation).
• Write research papers for publication in peer-reviewed scientific journals.
• Directly contribute to Flo’s scientific strategy by designing and planning future medical device studies and advising on global regulatory compliance requirements for new products.

Must Have

• PhD or Postdoc in Public Health, Reproductive Medicine, Population Health, Biostatistics, or other related fields.
• Direct experience of leading the design, execution, and data analysis of clinical research studies.
• Experience preparing documentation and supporting trials subject to FDA, EU MDR, or other global regulatory compliance bodies (Class II or higher).
• Strong working experience with data analysis and statistics (e.g. survival/lifetable analysis, linear and logistic regression, mixed models, etc.) in Python or/and R, including strong proficiency in writing complex SQL-queries.
• Strong publication record in peer-reviewed journals (as a first-author) and proven ability to write rigorous study protocols, statistical analysis plans, and scientific reports.

Nice to Have

• Working experience in projects related to Software as Medical Device (SaMD).
• Prior experience applying predictive models such as decision tree algorithms (e.g., CatBoost) or Bayesian networks.
• Experience of conducting systematic reviews and meta-analyses.
• You are meticulous but fast. We are a high-growth tech company. We need someone who can maintain academic-level precision at the speed of a scale-up.

How we work

We’re a mission-led, product-driven team. We move fast, stay focused and take ownership – from brief to build to impact. Debate is encouraged. Decisions are shared. We care about craft, ship with purpose, and always raise the bar.

You’ll be working with people who take their work seriously, not themselves. It takes commitment, resilience, and the drive to keep going when things get tough. Because better health outcomes are worth it.

What you\'ll get

We support impact with meaningful reward. Here’s what that looks like:

• Competitive salary and annual reviews
• Opportunity to participate in Flo’s performance incentive scheme
• Paid holiday, sick leave, and female health leave
• Enhanced parental leave and pay for maternity, paternity, same-sex and adoptive parents
• Accelerated professional growth through world-changing work and learning support
• Flexible office + home working, up to 2 months a year working abroad
• 5-week fully paid sabbatical at 5-year Floversary
• Flo Premium for friends & family, plus more health, pension and wellbeing perks

Diversity, equity and inclusion

Our strength is in our differences. At Flo, hiring is based on merit, skill and what you bring to the role – nothing else. We’re proud to be an equal opportunity employer, and we welcome applicants from all backgrounds, communities and identities. Read our privacy notice for job applicants.

Demographic Question

We invite applicants to share their demographic background. If you choose to complete this survey, your responses may be used to identify areas of improvement in our hiring process.

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