
Post Doctoral Scientist- Global Patient Safety Pharmacoepidemiology
- Indianapolis, IN
- $58,000-100,320 per year
- Permanent
- Full-time
- Develop a comprehensive understanding of common and emerging pharmacoepidemiologic methods and drive the adoption of a systematic methodological framework across the enterprise
- Accelerate the development of high-quality scientific protocols and strengthen the credibility of observational safety studies
- Increasing the acceptability of real-world evidence (RWE) for informing patient safety and regulatory decision-making.
- Leading and/or collaborating on the design, execution, and interpretation of pharmacoepidemiology studies
- Supporting the development and execution of risk management plans and specialized risk minimization activities.
- Identifying and evaluating potential safety signals and supporting communication with global regulatory authorities.
- Collaborating with cross-functional teams (e.g., regulatory, clinical development) to address research and regulatory questions
- Contributing to scientific publications, regulatory submissions, and conference presentations.
- Characterizing the natural history of diseases.
- A PhD or DrPH in epidemiology or other subject with high epidemiologic content
- Deep understanding in real-world data (RWD) and pharmacoepidemiologic methodologies, with the ability to design and execute epidemiological research, including the development of study protocols and statistical analysis plans.
- Competent in independent data analysis and interpretation of results from clinical and epidemiological studies.
- Highly motivated to learn new techniques while continually pursuing research and publication goals.
- Excellent computer skills; Knowledge of statistical software such as R, SAS, SPSS, Epi Info, and/or equivalent to digital tools support epidemiological research.
- Have strong analytic skills, oral and written communication skills, strong interpersonal and leadership skills, and able to work independently and collaboratively in multidisciplinary teams, strong problem-solving skills and the ability to apply pharmacoepidemiology principles to address a variety of complex research questions.
- This position is not permanent. It is for a fixed duration of two years with the potential to extend to 3 years. You may have opportunities to apply for full-time positions after your duration is complete.
- A writing sample will be requested during the interview process.
- Top industry research experience
- Mentoring by some of Lilly’s top scientists
- Collaboration and networking across dozens of postdoctoral scientists and other researchers