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

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London

Remote

GBP 125,000 - 150,000

Full time

4 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 offers the chance to lead innovative study designs and methodologies for regulatory and safety real-world evidence (RWE) studies, delivering impactful results. You will collaborate with experienced scientists and work with a diverse range of RWE studies, enhancing your skills and expertise in a supportive environment. If you are passionate about high-quality science and thrive in a client-facing role, this opportunity is perfect for you.

Qualifications

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

Responsibilities

  • Lead study design, methodology development, and result interpretation for RWE studies.
  • Conduct studies using electronic healthcare records, registries, and databases.

Skills

Epidemiology
Health Economics
Statistics
Drug Safety
Client Communication

Education

Masters in Epidemiology
PhD in Epidemiology
Masters in Health Economics
PhD in Health Economics

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 & Private sector considered).
  3. Drug safety experience, PAS studies, and external control arms - 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 while 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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