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Pharmacoepidemiologist (Safety) - client dedicated
Remote · United Kingdom or Stockholm, Stockholm, Sweden
Job Summary
Pharmacoepidemiologist (Safety) embedded in a client-partnered FSP, primarily remote in Europe with up to 20% travel to Belgium and the USA. Responsible for designing and executing pharmacoepidemiology studies addressing safety research questions across drug development, regulatory submissions, and marketed products. Activities include identifying methods, selecting data sources (RWD such as claims data, EHRs, registries, PAS), developing study concepts, protocols, and statistical analysis plans, and reporting findings. Collaborates with internal and external stakeholders, including RWE, Medical Affairs, Regulatory, HEOR, Clinical Development, and KOLs, to generate safety evidence, translate epidemiologic insights, and contribute to Integrated Evidence Generation Plans. Maintains compliance with GCP/GVP, communicates safety findings to stakeholders, and engages in continuous improvement and professional development. Travel up to 20% and work with a global team to enable safe and effective product development and lifecycle management.
Required Qualifications
- Background in health and life sciences (epidemiology, public health, MD, pharmD) or quantitative data sciences
- PhD in Epidemiology and/or pharmacoepidemiology or equivalent advantageous
- At least 5-year experience in epidemiology/pharmacoepidemiology
- Experience in drug safety
- Strong written and oral communication skills in English
- GCP and GVP knowledge
- Experience with RWE/D within pharmaceutical industry
- Ability to travel up to 20%
- Proven experience executing pharmacoepidemiology studies using real-world data
- Collaborative with strong communication and leadership skills
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