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

JR United Kingdom

Altrincham

Hybrid

GBP 50,000 - 90,000

Full time

7 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 implementation of real-world evidence studies, utilizing advanced methodologies to deliver high-quality results. You'll collaborate with a diverse team of scientists in a supportive environment that emphasizes mentorship and professional growth. Ideal candidates will have a strong academic background in Epidemiology or related fields, along with experience in drug safety and client-facing roles. This position offers the opportunity to make a significant impact in the field of public health and safety.

Qualifications

  • Masters or PhD in Epidemiology, Health Economics, or related field.
  • Experience in real-world evidence studies and drug safety.

Responsibilities

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

Skills

Epidemiology
Health Economics
Statistics
Drug Safety
Communication Skills

Education

Masters in Epidemiology
PhD in Epidemiology
Masters in Health Economics
Masters in Statistics

Job description

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

Client:

Evidencia Scientific Search and Selection Limited

Location:

Altrincham, United Kingdom

Job Category:

Other

EU work permit required:

Yes

Job Views:

9

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:

  1. Develop clear, scientifically sound RWE deliverables, including study designs, methodologies, results, and reports (e.g., study concept sheets, protocols, final reports, slide decks, manuscripts).
  2. Conduct real-world evidence studies using electronic healthcare records, registries, biobanks, and databases, utilizing global RWD sources.
  3. Implement advanced study designs including external comparators and quantitative bias analysis.

Ideal profile:

  1. Masters/PhD in Epidemiology, Health Economics, Statistics, or a related scientific discipline.
  2. Several years of experience in relevant RWE studies (backgrounds from Academia & Private sector considered).
  3. Drug safety experience, PAS studies, and external control arms are highly desirable.
  4. Passion for high-quality science and strong communication skills.
  5. 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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