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

JR United Kingdom

London

Hybrid

GBP 60,000 - 100,000

Full time

15 days ago

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An established industry player is on the lookout for a Senior Epidemiologist to join their Pharmacoepidemiology and Safety team. This role is pivotal in designing and implementing real-world evidence studies that deliver high-quality insights for regulatory and safety purposes. You will be responsible for developing scientifically sound methodologies and collaborating with a talented team of scientists. With a strong focus on mentorship and professional development, this position offers a unique opportunity to influence the future of healthcare research while working closely with Pharma clients. If you are passionate about science and eager to make an impact, this is the role for you.

Masters/PhD in Epidemiology, Health Economics, or Statistics required.
Experience in real-world evidence studies is essential.

Lead study design and methodology development for RWE studies.
Conduct studies using electronic healthcare records and global RWD sources.

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

Client: Evidencia Scientific Search and Selection Limited

Location: London, 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, 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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