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

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Leigh

Hybrid

GBP 50,000 - 90,000

Full time

4 days ago
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Job summary

Join a forward-thinking company as a Senior Epidemiologist, where you will lead the design and execution of real-world evidence studies. This role offers the opportunity to develop scientifically sound deliverables and collaborate with a team of experienced scientists. You will engage with Pharma clients, utilizing your expertise in epidemiology and health economics to deliver high-quality evidence. With a structured onboarding process and excellent mentorship opportunities, this position is perfect for those passionate about advancing their career in a supportive environment. Make a meaningful impact in the field of pharmacoepidemiology and safety.

Qualifications

  • Several years of experience in relevant RWE studies from Academia or Private sector.
  • Drug safety experience and consulting/client-facing experience with Pharma clients are desirable.

Responsibilities

  • Lead study design and methodology development for regulatory and safety RWE studies.
  • Conduct real-world evidence studies using global RWD sources.

Skills

Epidemiology
Health Economics
Statistics
Drug Safety
Communication Skills

Education

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

Tools

Electronic Healthcare Records
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 & 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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