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

JR United Kingdom

Bury

Hybrid

GBP 50,000 - 80,000

Full time

18 days ago

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Job summary

An established industry player is seeking a Senior Epidemiologist to join their Pharmacoepidemiology and Safety team. This role involves leading the design and execution of real-world evidence studies, ensuring high-quality deliverables that meet client needs. You will collaborate with experienced scientists and engage directly with Pharma clients, enhancing your skills in a supportive environment. The company offers a structured onboarding process and excellent mentorship opportunities, making it an ideal place for passionate professionals looking to thrive in the field of epidemiology. Join a dynamic team and make a meaningful impact in healthcare research!

Qualifications

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

Responsibilities

  • Lead study design and methodology development for RWE studies.
  • Conduct studies using global RWD sources and implement advanced designs.

Skills

Epidemiology
Health Economics
Statistics
Communication Skills
Drug Safety
Consulting

Education

Masters in Epidemiology
PhD in Epidemiology

Tools

Electronic Healthcare Records
Biobanks
Databases

Job description

Social network you want to login/join with:

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

Evidencia Scientific Search and Selection Limited

Location:

bury, United Kingdom

Job Category:

Other

EU work permit required:

Yes

Job Views:

8

Posted:

18.04.2025

Expiry Date:

02.06.2025

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, 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 - 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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