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Senior Epidemiologist - Pharmacoepidemiology & Safety (RWE) - London / hybrid / remote
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Ashton-under-Lyne
Remote
GBP 50,000 - 90,000
Full time
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Job summary
An established industry player is on the lookout for a Senior Epidemiologist to join their dynamic Pharmacoepidemiology and Safety team. This role offers the opportunity to lead innovative study designs and methodologies, ensuring the delivery of high-quality real-world evidence for regulatory and safety studies. You will collaborate with a diverse team of experienced scientists, enhancing your skills and knowledge while contributing to impactful projects. With a structured onboarding process and excellent mentorship opportunities, this position is perfect for those passionate about advancing science in a supportive environment. If you are driven and eager to make a difference, this role is for you.
Qualifications
- Several years of experience in relevant RWE studies, both in Academia and Private sector.
- Strong communication skills and a passion for high-quality science.
Responsibilities
- Lead study design and methodology development for regulatory and safety RWE studies.
- Conduct real world evidence studies using electronic healthcare records and databases.
Skills
Education
Job description
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/development opportunities.
For more information, apply now or reach me at greg.harris@evisci.com
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