Data Scientist - Real-World Evidence Analyst

Bebeepharmaceutical; A distancia; MXN 911,000 - 1,276,000; Jornada completa

Descripción de la vacante

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.

Servicios

Fully remote work environment

Flexible schedules

Tailored development programs

Formación

• 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.

Responsabilidades

• 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.

Conocimientos

Statistical analysis

Data management

Regulatory submissions

R

Python

SAS

SQL

Educación

Ph.D. or M.S. in Statistics or related field

Descripción del empleo

Job Title

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.

Key Responsibilities

• 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.

Requirements

• 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.

Why Choose Us?

• 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