Senior Clinical Data Engineer — LATAM Global Trials

Precision Medicine Group

United States

Remote

USD 120.000 - 180.000

Vollzeit

14 Tage+

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Zusammenfassung

Precision Medicine Group is expanding its data engineering capabilities and seeks a Senior Clinical Data Engineer to build and optimize clinical data systems across global trials. You will lead data standardization, validation frameworks, and scalable databases and pipelines, with a focus on regulatory compliance.

You will mentor junior engineers, implement SAS-based workflows, and collaborate with Biostatistics, Clinical Operations, and Regulatory Affairs to translate clinical requirements into

Qualifikationen

  • Minimum 6 years in clinical monitoring, trials, or equivalent.
  • Advanced programming and automation skills; database design; dashboard development; CDISC governance.
  • Professional working proficiency in English.

Aufgaben

  • Lead development and optimization of clinical data systems across global trials.
  • Design data standardization strategies and validation frameworks.
  • Architect modular SAS codebases and mentor junior engineers.
  • Ensure regulatory alignment with GCP and FDA 21 CFR Part 11.
  • Develop dashboards and analytics tools for real-time insights.
  • Collaborate with Biostatistics, Clinical Operations, Regulatory Affairs.

Kenntnisse

SAS programming
Python
SQL
Data standardization
Data governance
Dashboard development
Regulatory compliance

Ausbildung

Bachelor’s Degree in life sciences, data science, or related field

Tools

SAS

Jobbeschreibung

Precision Medicine Group is expanding its data engineering capabilities and seeks a Senior Clinical Data Engineer to build and optimize clinical data systems across global trials. You will lead data standardization, validation frameworks, and scalable databases and pipelines, with a focus on regulatory compliance.

You will mentor junior engineers, implement SAS-based workflows, and collaborate with Biostatistics, Clinical Operations, and Regulatory Affairs to translate clinical requirements into

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