Senior Clinical Data Engineer — Remote & Regulatory‑Focused

Precision Medicine Group; Colombia; Presencial; COP 372.902.000 - 559.354.000; Jornada completa

Descripción de la vacante

Precision Medicine Group in Colombia seeks a Senior Clinical Data Engineer to lead the design, development, and optimization of clinical data systems across global trials. You'll drive data standardization, validation frameworks, scalable databases, and ETL pipelines, with a focus on regulatory compliance (GCP, 21 CFR Part 11) and audit trails.

You will mentor juniors and collaborate with Biostatistics, Clinical Operations, and Regulatory Affairs teams.

Formación

• Bachelor’s Degree in life sciences, statistics, data management, or related field.
• Minimum 6 years of clinical data management or related experience.
• Strong SAS programming, with Python/R/SQL preferred.
• Professional proficiency in English.

Responsabilidades

• Lead enterprise-level data standardization and mapping across programs to enable analytics.
• Design and implement robust validation frameworks for data quality and integrity.
• Architect and maintain modular SAS codebases for complex data workflows; mentor juniors.
• Ensure compliance with GCP, FDA 21 CFR Part 11; establish audit trails and documentation.
• Develop dashboards and analytics tools to monitor data quality and trial progress.
• Collaborate with Biostatistics, Clinical Operations, and Regulatory Affairs to deliver study data solutions.
• Design secure, high-performance relational databases and data lakes; optimize queries.

Conocimientos

SAS programming

Python

R

SQL

Data modeling

Educación

Bachelor’s Degree in life sciences / statistics / data management or related field

Herramientas

SAS

Python

R

SQL

ETL

Descripción del empleo

Precision Medicine Group in Colombia seeks a Senior Clinical Data Engineer to lead the design, development, and optimization of clinical data systems across global trials. You'll drive data standardization, validation frameworks, scalable databases, and ETL pipelines, with a focus on regulatory compliance (GCP, 21 CFR Part 11) and audit trails.

You will mentor juniors and collaborate with Biostatistics, Clinical Operations, and Regulatory Affairs teams.