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Senior Epidemiologist - Pharmacoepidemiology & Safety (RWE) - London / hybrid / remote

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Leeds

Remote

GBP 40,000 - 80,000

Full time

11 days ago

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Job summary

An established industry player is looking for a Senior Epidemiologist to join their Pharmacoepidemiology and Safety team. This role involves leading study design and methodology development for regulatory and safety RWE studies, ensuring high-quality evidence delivery. You will have the opportunity to work with a large team of experienced scientists and engage in a structured onboarding process designed for long-term success. This position not only offers a chance to contribute to impactful studies but also provides excellent mentorship and development opportunities in a collaborative environment. If you have a passion for high-quality science and strong communication skills, this is the perfect opportunity for you.

Qualifications

  • Several years of experience in relevant RWE studies, ideally with drug safety.
  • Masters/PhD in Epidemiology, Health Economics, or Statistics required.

Responsibilities

  • Develop scientifically sound RWE deliverables including study designs and reports.
  • Conduct real-world evidence studies utilizing global RWD sources.

Skills

Epidemiology
Health Economics
Statistics
Drug Safety
Communication Skills

Education

Masters in Epidemiology
PhD in Epidemiology

Tools

Electronic Healthcare Records
Registries
Biobanks
Databases

Job description

Job Description

Senior Epidemiologist - Pharmacoepidemiology & Safety (RWE) - London / fully remote considered

My client is seeking a passionate and detail-oriented professional to join their Pharmacoepidemiology and Safety team. In this role, you will lead study design, methodology development, and result interpretation for regulatory and safety RWE studies, delivering high-quality evidence to meet client needs.

Role/scope:

  1. Develop clear, scientifically sound RWE deliverables, including study designs, methodologies, results, and reports (e.g., study concept sheets, protocols, final reports, slide decks, manuscripts).
  2. Conduct real-world evidence studies using electronic healthcare records, registries, biobanks, and databases, utilizing global RWD sources.
  3. Implement advanced study designs including external comparators and quantitative bias analysis.

Ideal profile:

  1. Masters/PhD in Epidemiology, Health Economics, Statistics, or a related scientific discipline.
  2. Several years of experience in relevant RWE studies (backgrounds from academia and the private sector considered).
  3. Drug safety experience, PAS studies, and external control arms are highly desirable.
  4. Passion for high-quality science and strong communication skills.
  5. Consulting/client-facing experience working directly with Pharma clients is highly desirable.

You'll be joining a company with a very structured and concise onboarding, shadowing, and settling-in period, setting people up for long-term success. You will also be able to collaborate with a large team of experienced scientists, developing your knowledge and skills, covering a broad scope of RWE studies. You'll be part of a small specialist team within this group and play a key role in a growing offering with excellent mentorship/development opportunities.

For more information, apply now or reach me at greg.harris@evisci.com

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