Epidemiologist

KEMIO Consulting; United Kingdom; A distancia; Jornada completa

Descripción de la vacante

A healthcare data analytics organization is seeking an experienced Epidemiologist to join their team in the UK. You will design and deliver observational studies for rare diseases and oncology, collaborating with biostatistical teams and pharma clients. The ideal candidate has a PhD in Epidemiology and at least 2 years of relevant experience. Strong statistical skills and written communication proficiency are essential, alongside a passion for impactful real-world evidence generation.

Formación

• 2+ years' experience in RWE, epidemiology, HEOR, or pharmacoepidemiology role.
• Proven ability to design and write protocols for observational studies.
• Strong written communication skills across various formats.

Responsabilidades

• Develop high-quality study protocols and analysis plans for RWE studies.
• Design observational studies using diverse RWD sources.
• Serve as a scientific point of contact for pharmaceutical clients.

Conocimientos

Design study protocols

Statistical analysis

Written communication

Educación

PhD in Epidemiology or related field

Descripción del empleo

Join to apply for the Epidemiologist role at KEMIO Consulting

Location: UK (Remote)

Employment: Permanent

Experience: 2yrs +

KEMIO Consulting is working closely with a RWE and Healthcare Data Analytics organisation to find an experienced PhD qualified Epidemiologist to join their expanding team delivering high-quality Real-World Evidence (RWE) studies to global pharma and biotech partners.

In this role, you will support on the design and delivery of observational studies across rare diseases and oncology, partnering closely with internal biostatistical teams and external pharmaceutical/biotech clients.

You’ll shape and review study protocols, ensure methodological rigour, interpret complex data, and communicate insights that influence clinical, regulatory, and market decisions.

Key Responsibilities

• Develop high-quality study protocols, analysis plans, and methodological frameworks for RWE studies.
• Design observational, retrospective, and prospective studies using diverse RWD sources (registries, EMR, claims, disease-specific datasets).
• Work closely with biostatistical teams to inform sample size assumptions, modelling approaches, and analysis structures.
• Translate scientific questions into analytical specifications and validate statistical outputs.
• Serve as a scientific point of contact for pharmaceutical and biotech clients.
• Present study proposals, methods, and results in a clear, credible, and engaging way.
• Support business development through scientific input into proposals and client discussions.
• Interpret results, draft reports, and contribute to manuscripts, conference abstracts, and publications.

Experience & Qualifications

• PhD in Epidemiology, Public Health, Biostatistics, or related field.
• 2+ years' experience in an RWE, epidemiology, HEOR, or pharmacoepidemiology role.
• Proven ability to design and write protocols for observational studies.
• Understanding of advanced epidemiological methods (e.g., causal inference, propensity methods, survival analysis).
• Experience interacting with biostatistical teams and cross-functional collaborators.
• Client-facing experience with pharmaceutical, biotech, or health research partners.
• Strong written communication skills (reports, abstracts, publications).

Preferred

• Experience in rare diseases, oncology, or chronic disease research.
• Familiarity with global regulatory/HTA evidence requirements.
• Exposure to RWD such as claims, EMR, registries, or bespoke disease datasets.
• Experience in a small/medium consultancy or agile research organisation.

If you are passionate about generating rigorous, meaningful evidence that will transform real‑world data into impactful insights that improve outcomes for patients, we’d love to speak with you.