Enable job alerts via email!

Senior Epidemiologist (Pharma/Drug Safety) - Highly Scientific Mid-sized Healthcare Consultancy

Evidencia Scientific Search and Selection Limited

Greater London

Hybrid

GBP 80,000 - 100,000

Full time

30+ days ago

Boost your interview chances

Create a job specific, tailored resume for higher success rate.

Job summary

Join a forward-thinking healthcare consultancy as a Senior Epidemiologist, where your expertise in Pharmacoepidemiology and drug safety will be pivotal in leading real-world evidence studies. This role offers the chance to develop scientifically robust methodologies and collaborate with a diverse team of experienced scientists. You'll have the opportunity to impact healthcare decisions by delivering high-quality evidence while benefiting from a structured onboarding process and a supportive work environment. If you're passionate about high-quality science and eager to contribute to meaningful projects, this position is perfect for you.

Qualifications

  • 5+ years experience in relevant RWE studies, with a focus on drug safety.
  • Strong background in study design and methodology development.

Responsibilities

  • Lead study design and methodology for regulatory and safety RWE studies.
  • Deliver scientifically sound RWE deliverables and reports.

Skills

Pharmacoepidemiology
Drug Safety
Statistical Analysis
Communication Skills

Education

Masters in Epidemiology
PhD in Epidemiology
Health Economics
Statistics

Tools

Electronic Healthcare Records
Biobanks
Databases

Job description

Senior Epidemiologist (Pharma/Drug Safety) - Highly Scientific Mid-sized Healthcare Consultancy

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:

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

Ideal profile:

  • Masters/PhD in Epidemiology, Health Economics, Statistics, or a related scientific discipline.
  • 5+ years of experience in relevant RWE studies (backgrounds from academia and the private sector considered).
  • Drug safety experience, PAS studies, and external control arms are highly desirable.
  • A passion for high-quality science and strong communication skills.

You'll be joining a company with a structured and concise onboarding process, shadowing, and settling-in period, setting you up for long-term success. You will also 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.

Seniority level

Mid-Senior level

Employment type

Full-time

Job function

Management, Consulting, and Science

Industries

Staffing and Recruiting

Get your free, confidential resume review.
or drag and drop a PDF, DOC, DOCX, ODT, or PAGES file up to 5MB.