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Pharmacoepidemiologist

Cpl Life Sciences
Posted 15 hours ago, valid for a month
Location

London, Greater London EC1R 0WX

Contract type

Full Time

In order to submit this application, a Reed account will be created for you. As such, in addition to applying for this job, you will be signed up to all Reed’s services as part of the process. By submitting this application, you agree to Reed’s Terms and Conditions and acknowledge that your personal data will be transferred to Reed and processed by them in accordance with their Privacy Policy.

Sonic Summary

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  • The position is for a Pharmacoepidemiologist on a 12-month contract, fully remote, open to candidates in the UK and Netherlands.
  • The role involves supporting the evaluation of medicine safety by analyzing data from clinical research and health databases.
  • Candidates must have a PhD in Epidemiology or a related field, along with experience in cross-functional teams within the pharmaceutical industry.
  • A strong background in epidemiology research, experience reviewing safety data from clinical trials, and familiarity with large health databases are essential.
  • The position offers a competitive daily rate, but specific salary details are not provided.

Pharmacoepidemiologist – 12-month Contract

Location: Fully remote (open to candidates in the UK and Netherlands)

Interview: One stage process

Rate: Competitive daily rate

We’re looking for a Pharmacoepidemiologist to join a global pharmaceutical company’s Pharmacovigilance team. In this role, you’ll support the evaluation of medicine safety across multiple treatment areas by reviewing and analysing data from clinical research, scientific literature, and large health databases.

You’ll work closely with senior experts and collaborate with teams across Medical and Development, gaining valuable exposure to drug development, safety monitoring, and reporting processes.

  • Review, interpret, and summarise safety data from published observational studies and clinical trials.
  • Work with the Statistical and Real-World Data (RWD) Science team to analyse electronic health data (including health insurance claims and EHR data) to uncover additional safety insights.
  • Collaborate with senior epidemiologists and cross-functional teams across Medical and Development, gaining valuable exposure to the broader drug development and safety monitoring process.

Key requirements are:

  • PhD (or equivalent) in Epidemiology or related field
  • Experience working in cross-functional teams in pharma or similar industries
  • Strong background in epidemiology research and cohort studies
  • Skilled in key analysis methods, including time-to-event analysis
  • Knowledge of group comparison methods (e.g., propensity scores)
  • Experience reviewing safety data from clinical trials
  • Familiarity with large US and international health databases (e.g., insurance claims, electronic health records)
  • Interest or experience in using new tools/technologies to enhance literature reviews

If this role is of interest please apply direct or email for a further conversation

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In order to submit this application, a Reed account will be created for you. As such, in addition to applying for this job, you will be signed up to all Reed’s services as part of the process. By submitting this application, you agree to Reed’s Terms and Conditions and acknowledge that your personal data will be transferred to Reed and processed by them in accordance with their Privacy Policy.