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

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Altrincham

Remote

GBP 50,000 - 90,000

Full time

4 days ago
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Job summary

Join a forward-thinking company as a Senior Epidemiologist, where you will lead innovative studies in Pharmacoepidemiology and Safety. This role offers the opportunity to develop scientifically sound deliverables and conduct impactful real-world evidence studies. Collaborate with a dedicated team of scientists, enhancing your skills in a supportive environment focused on mentorship and professional growth. If you are passionate about high-quality science and have a strong background in drug safety and RWE studies, this position is perfect for you. Embrace the chance to make a significant impact in the field and advance your career.

Qualifications

  • Masters/PhD in Epidemiology, Health Economics, or related field required.
  • Several years of experience in real-world evidence studies preferred.

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

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

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.
  • Utilize 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/development opportunities.

For more information, apply now or reach me at greg.harris@evisci.com

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