Senior Clinical Data Engineer – LATAM

This is a fully remote position, open to applicants in Argentina, +3 more countries.

📋 Description

• Oversee the creation and enhancement of clinical data systems that ensure regulatory compliance, facilitate advanced analytics, and promote operational excellence throughout global trials.

• Lead initiatives for enterprise-level data standardization and manage data standards across various programs.

• Design and implement scalable frameworks for validation to identify and rectify systemic data issues.

• Develop and maintain modular SAS codebases while establishing coding standards.

• Provide mentorship to junior engineers in areas such as automation, reproducibility, and performance optimization.

• Spearhead compliance initiatives related to GCP, FDA 21 CFR Part 11, and international regulatory requirements.

• Establish documentation protocols and supervise audit trail governance.

• Create dynamic dashboards and analytics tools to deliver real-time insights into data quality, trial progress, and operational KPIs.

• Convert complex datasets into actionable intelligence for clinical and regulatory stakeholders.

• Collaborate with Biostatistics, Clinical Operations, and Regulatory Affairs teams.

• Transform clinical and scientific requirements into scalable technical solutions.

• Lead the design and optimization of secure, high-performance relational databases and data lakes.

• Integrate data from various clinical systems using ETL pipelines.

⛳️ Requirements

• Bachelor’s Degree in a relevant discipline (life sciences, statistics, data management, clinical operations) or a relevant/equivalent combination of education, training, and experience.

• At least 6 years of experience in clinical monitoring, clinical trial management, or a similar role.

• Proficient in advanced programming and automation techniques; experience in database design, dashboard development, and CDISC governance.

• Professional working proficiency in English.

• Strong oral and written communication skills.

• Exceptional organizational and time management abilities.

• Capable of working both collaboratively within a team and independently as needed.

• Skilled at extracting relevant information from protocols, electronic study data systems, and clinical systems.

• Proficient in statistical analysis and monitoring tools for data.

• Detail-oriented with robust analytical and problem-solving capabilities.

• Proven experience in integrated risk planning and management.

• Ability to mentor junior team members effectively.

• Experience working with large, complex datasets sourced from multiple locations.

• Knowledge of data governance, privacy, and security best practices in the realm of clinical research.

• Preferred: Experience as a Clinical Data Engineer or Programmer in a Contract Research Organization (CRO).

• Preferred: Familiarity with automation and AI Agent Deployment in regulated environments.

🏝️ Benefits

• Competitive salary and performance-based incentives.

• Comprehensive health, dental, and vision insurance.

• Opportunities for professional development and continuous learning.

• Flexible working arrangements and a supportive work environment.