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Data Scientist - Real-World Evidence Analyst
Job summary
A leading pharmaceutical company in Mexico is seeking a Principal Statistician skilled in Biostatistics and passionate about Real-World Evidence (RWE). This role involves designing statistical analyses, leading RWE studies, and supporting global regulatory submissions. The ideal candidate should hold a Ph.D. or M.S. in Statistics, possess strong programming skills in R, Python, SAS, and SQL, and have at least 5 years of pharmaceutical industry experience. Enjoy a fully remote work environment, career progression opportunities, and a collaborative team culture.
Benefits
Qualifications
- At least 5 years of experience in the pharmaceutical industry.
- Proven experience in RWE/RWD analytics and regulatory submissions.
- Strong understanding of causal inference and survival analysis.
Responsibilities
- Design and execute statistical analyses for regulatory submissions.
- Lead RWE study design for pharmaceutical companies.
- Develop and validate models to analyze complex datasets.
- Support regulatory submissions by communicating insights.
Skills
Education
Principal Statistician
We are seeking an experienced Biostatistician with a passion for Real‑World Evidence (RWE) and Real‑World Data (RWD).
The ideal candidate will have a strong background in statistical analysis, data management, and regulatory submissions.
- Design and execute statistical analyses using EHR, claims, registry, and observational data to support regulatory submissions and inform business decisions.
- Lead RWE study design, including retrospective and pragmatic trials, to generate high‑quality evidence for pharmaceutical companies.
- Develop and validate models using programming languages such as R, Python, SAS, and SQL to analyze complex datasets.
- Support regulatory submissions to global authorities, such as the FDA and EMA, by communicating insights and results to cross‑functional teams.
- A Ph.D. or M.S. in Statistics, Biostatistics, or a related field, with at least 5 years of experience in the pharmaceutical industry.
- Proven experience in RWE/RWD analytics and regulatory submissions, with a strong understanding of causal inference, survival analysis, and longitudinal data.
- Strong programming skills in R, Python, SAS, and SQL, as well as experience with data management tools.
- Familiarity with CDISC standards such as SDTM, ADaM, and CDASH, and ICH GCP guidelines.
- We offer a fully remote work environment with flexible schedules, allowing you to maintain a healthy work‑life balance.
- You’ll collaborate with a global team of experts in the pharmaceutical industry, contributing to innovative therapies and meaningful healthcare outcomes.
- Tailored development programs and career‑progression opportunities ensure your continued growth and success.
If you're a skilled Biostatistician passionate about making data matter, we encourage you to apply today!
Keywords: Biostatistics, Real‑World Evidence, RWE, Real‑World Data, RWD, Pharmaceutical Statistics, Healthcare Analytics, Statistical Analysis, Data Management, Regulatory Submissions, Pharmaceutical Industry
* The salary benchmark is based on the target salaries of market leaders in their relevant sectors. It is intended to serve as a guide to help Premium Members assess open positions and to help in salary negotiations. The salary benchmark is not provided directly by the company, which could be significantly higher or lower.