Senior Clinical Data Engineer — Global Trials & Data Platform

Precision For Medicine; Argentina; On-site; ARS 1,500,000 - 2,100,000; Full time

Job summary

Precision Medicine Group is hiring a Senior Clinical Data Engineer to lead global clinical data systems, standardization, and validation within a growing regional function spanning Latin America and beyond.

You will architect high-performance databases and ETL pipelines, ensure regulatory compliance (GCP, FDA 21 CFR Part 11), mentor junior engineers, and partner with Biostatistics, Clinical Operations, and Regulatory Affairs to deliver actionable insights.

Qualifications

• Bachelor’s degree in a life sciences, statistics, data management, or related field.
• Minimum 6 years of clinical data experience in trials or equivalent.
• Advanced programming, automation, dashboard development, and CDISC governance.
• Professional working proficiency in English.

Responsibilities

• Lead data standardization and mapping strategies across programs.
• Design and implement scalable data quality validation frameworks.
• Architect modular SAS-based data pipelines; mentor junior engineers.
• Ensure regulatory alignment with GCP and FDA 21 CFR Part 11.
• Develop dynamic dashboards to provide real-time trial insights.
• Collaborate with Biostatistics, Clinical Operations, and Regulatory Affairs.
• Design secure, high-performance databases and data lakes.

Skills

SAS programming

SQL

Python

Data standardization

Data quality

Regulatory compliance

English proficiency

Education

Bachelor's degree in life sciences/statistics/related field

Tools

SAS

Python

R

Job description

Precision Medicine Group is hiring a Senior Clinical Data Engineer to lead global clinical data systems, standardization, and validation within a growing regional function spanning Latin America and beyond.

You will architect high-performance databases and ETL pipelines, ensure regulatory compliance (GCP, FDA 21 CFR Part 11), mentor junior engineers, and partner with Biostatistics, Clinical Operations, and Regulatory Affairs to deliver actionable insights.