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

JR United Kingdom

Bolton

Hybrid

GBP 60,000 - 80,000

Full time

15 days ago

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Job summary

An innovative firm is seeking a Senior Epidemiologist to lead impactful RWE studies. This role involves designing scientifically sound studies, utilizing global data sources, and delivering high-quality evidence for regulatory needs. You'll collaborate with a dedicated team of experts, benefiting from structured onboarding and mentorship, while contributing to a growing field of pharmacoepidemiology and safety. If you're passionate about high-quality science and have a strong background in epidemiology or health economics, this opportunity offers a chance to make a significant impact in the industry.

Qualifications

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

Responsibilities

  • Lead study design and methodology development for regulatory RWE studies.
  • Conduct real-world evidence studies using electronic healthcare records.

Skills

Epidemiology
Health Economics
Statistics
Drug Safety
Communication Skills

Education

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

Job description

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Senior Epidemiologist - Pharmacoepidemiology & Safety (RWE) - London / hybrid / remote, Bolton, Greater Manchester
Client:

Evidencia Scientific Search and Selection Limited

Location:

Bolton, Greater Manchester, United Kingdom

Job Category:

Other

EU work permit required:

Yes

Job Views:

4

Posted:

13.04.2025

Expiry Date:

28.05.2025

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:

  • 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, or Statistics or a related scientific discipline.
  • Several years of experience in relevant RWE studies (backgrounds from Academia & Private sector considered).
  • Drug safety experience, PAS studies, and external control arms are highly desirable.
  • Passion for high-quality science and strong communication skills.
  • 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 and development opportunities.

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