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

JR United Kingdom

Bury

Remote

GBP 40,000 - 80,000

Full time

3 days ago
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Job summary

Join a forward-thinking company as an Epidemiologist in Pharmacoepidemiology and Safety, where you will lead innovative real-world evidence studies. This role offers the chance to develop scientifically sound deliverables and collaborate with a team of experienced scientists. With a structured onboarding process and a focus on high-quality science, you will thrive in a supportive environment that encourages professional growth. If you are passionate about epidemiology and have a strong background in RWE studies, this opportunity is perfect for you to make a significant impact in the field.

Qualifications

  • 2+ years of experience in relevant RWE studies, including drug safety.
  • Masters/PhD in Epidemiology or related field required.

Responsibilities

  • Lead study design and methodology development for RWE studies.
  • Conduct real-world evidence studies using various data 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

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

Evidencia Scientific Search and Selection Limited

Location:

bury, United Kingdom

Job Category:

Other

EU work permit required:

Yes

Job Description:

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. Utilize 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. 2+ years of experience in relevant RWE studies (backgrounds from Academia & Private sector considered).
  3. Drug safety experience, PAS studies, external control arms - highly desirable.
  4. Passion for high-quality science and strong communication skills.

You'll be joining a company with a structured 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 across a broad scope of RWE studies.

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

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