Senior Clinical Data Engineer – LATAM

🔥 1 hour ago

🌐 Argentina, Brazil, +2 more countries – Remote

🇦🇷 Argentina – Remote 🇧🇷 Brazil – Remote 🇨🇴 Colombia – Remote 🇲🇽 Mexico – Remote

⏰ Full Time

🟠 Senior

🚰 Data Engineer

👻 Ghost score 19%

What it means: how likely this posting is sitting open without active hiring.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.How we score it: age, reposts, open roles vs team size, how fast jobs close, and whether pay is listed.Fine print: an estimate from public data, not a judgment of the company. Real jobs can score high, so treat it as a hint, not a fact.

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Precision Medicine Group

WebsiteLinkedInAll Job Openings

1001 - 5000 employees

Founded 2012

💼 Consulting

🏥 Healthcare

📦 Logistics

💰 $35.2M Venture Round on 2021-03

Consulting • Healthcare • Logistics

Precision Medicine Group is a global team of experts that specializes in precision medicine, which combines advanced lab sciences, translational informatics, regulatory affairs, payer insights, and marketing communications. The company focuses on overcoming product development and commercialization challenges for pharmaceutical and life sciences clients. Their services include biomarker-driven research and development, as well as commercialization support for life science organizations from launch to product maturity. Precision Medicine Group operates through two main arms: Precision for Medicine and Precision AQ, specializing in clinical and commercial solutions respectively.

📋 Description

• Lead the development and optimization of clinical data systems supporting regulatory compliance, advanced analytics, and operational excellence across global trials • Drive enterprise-level data standardization initiatives and govern data standards across programs • Design and implement scalable validation frameworks to detect and resolve systemic data issues • Architect and maintain modular SAS codebases and establish coding standards • Mentor junior engineers in automation, reproducibility, and performance optimization • Lead compliance initiatives for GCP, FDA 21 CFR Part 11, and global regulatory requirements • Define documentation protocols and oversee audit trail governance • Develop dynamic dashboards and analytics tools for real-time insights into data quality, trial progress, and operational KPIs • Translate complex datasets into actionable intelligence for clinical and regulatory stakeholders • Liaise with Biostatistics, Clinical Operations, and Regulatory Affairs • Translate clinical and scientific requirements into scalable technical solutions • Lead design and optimization of secure, high-performance relational databases and data lakes • Integrate data from diverse clinical systems through ETL pipelines

🎯 Requirements

• Bachelor’s Degree in a relevant field (life sciences, statistics, data management, clinical operations) or relevant/equivalent combination of education, training, and experience • Minimum 6 years experience in clinical monitoring, clinical trial management or equivalent • Advanced programming and automation skills; database design; dashboard development; CDISC governance • Professional working proficiency in English • Highly effective oral and written communication skills • Excellent organizational and time management skills • Ability to work in a team or independently as required • Ability to extract pertinent information from protocols, electronic study data systems and clinical systems • Proficiency in statistical analysis and data monitoring tools • Detail-oriented with strong analytical and problem-solving skills • Demonstrated experience with integrated risk planning & management • Ability to mentor junior team members • Ability to work with large, complex datasets from multiple sources • Knowledge of data governance, privacy, and security best practices in clinical research • Preferred: CRO experience as a Clinical Data Engineer or Programmer • Preferred: Automation and AI Agent Deployment in Regulated Environments