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

JR United Kingdom

Leeds

Hybrid

GBP 40,000 - 80,000

Full time

15 days ago

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An established industry player is seeking a Senior Epidemiologist to join their Pharmacoepidemiology and Safety team. This role offers the opportunity to lead the design and implementation of real-world evidence studies, ensuring high-quality deliverables that meet client needs. You'll collaborate with experienced scientists and be part of a structured onboarding process that sets you up for long-term success. With a focus on mentorship and professional development, this position is ideal for those passionate about advancing their career in epidemiology and drug safety. If you thrive in a dynamic environment and are eager to make a significant impact, this role is for you.

Masters/PhD in Epidemiology or related field required.
Several years of experience in RWE studies is essential.

Lead study design and methodology development for RWE studies.
Conduct studies using electronic healthcare records and databases.

Epidemiology

Health Economics

Statistics

Drug Safety

Communication Skills

Masters in Epidemiology

PhD in Epidemiology

Relevant scientific discipline

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Senior Epidemiologist - Pharmacoepidemiology & Safety (RWE) - London / hybrid / remote, Leeds, West Yorkshire

Client:

Evidencia Scientific Search and Selection Limited

Location:

Leeds, West Yorkshire, United Kingdom

Job Category:

Other

EU work permit required:

Yes

Job Views:

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, Statistics, or 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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