We're expanding our data engineering capabilities across Mexico, Brazil, Argentina, Colombia, Chile, and Peru, and we're hiring a Senior Clinical Data Engineer to help build the foundation of this new regional function.
In this role, you'll lead the development and optimization of clinical data systems, drive data standardization, build validation frameworks, and design high‐performance databases and pipelines across general trials.
The Senior Clinical Data Engineer leads the strategic development and optimization of clinical data systems to support regulatory compliance, advanced analytics, and operational excellence across global trials.
This role drives enterprise-level data standardization initiatives, and architects scalable validation frameworks to proactively address systemic data issues.
With deep expertise in Python, R, SQL, and SAS, the engineer builds and maintains modular codebases, sets coding standards, and mentors junior engineers.
The role also oversees regulatory alignment with GCP and FDA 21 CFR Part 11, establishing robust documentation and audit trail protocols.
Through dynamic dashboards and analytics tools, the engineer delivers actionable insights into trial performance and data quality.
As a strategic liaison across Biostatistics, Clinical Operations, and Regulatory Affairs, the engineer translates clinical requirements into scalable technical solutions and leads the design of secure, high‐performance databases and ETL pipelines integrating data from diverse clinical systems.
Essential functions of the job include but are not limited to:
Data Standardization & Mapping
Spearhead the development of enterprise-level data mapping strategies that transform raw clinical data into standardized formats for high-impact analytics.
Lead the adoption and governance of data standards across programs to ensure regulatory alignment and consistency.
Data Quality Assurance
Design and implement robust, scalable validation frameworks that proactively detect and resolve systemic data issues.
Serve as a strategic partner to Clinical Data Managers and cross-functional teams, driving continuous improvement in data integrity across global trials.
Programming & Scripting
Architect and maintain advanced, modular codebases using Python, R, SQL, and SAS to support complex data engineering workflows.
Establish coding standards and mentor junior engineers in automation, reproducibility, and performance optimization.




Example use cases include edit checks, reconciliations, exception listings, programmed protocol deviations, and resource projections based on site data entry volume.
Regulatory Compliance & Documentation
Lead compliance initiatives to ensure all data systems and workflows meet GCP, FDA 21 CFR Part 11, and evolving global regulatory requirements.
Define documentation protocols and oversee audit trail governance to support inspection readiness and transparency.
Reporting & Visualization
Develop and operationalize dynamic dashboards and analytics tools that provide real-time insights into data quality, trial progress, and operational KPIs.
Translate complex datasets into actionable intelligence for clinical and regulatory stakeholders.
Collaboration & Cross-Functional Support
Act as a strategic liaison between Clinical Data Engineering and Biostatistics, Clinical Operations, and Regulatory Affairs.
Translate clinical and scientific requirements into scalable technical solutions that support study execution and data delivery.
Database Design & Optimization
Lead the design and optimization of secure, high-performance relational databases and data lakes.
Ensure infrastructure scalability, query efficiency, and data governance for large-scale clinical datasets.
Qualifications
Minimum Required
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
Other Required
Highly effective oral and written communication skills with the ability to communicate effectively with project team members
Excellent organizational and time management skills
Ability to work in a team or independently as required




Demonstrated ability to learn how 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
Preferred
CRO experience as a Clinical Data Engineer or Programmer
Skills
Strong analytical and problem-solving skills with attention to data quality and integrity
Ability to work with large, complex datasets from multiple sources
Effective communication skills to collaborate with cross-functional teams
Knowledge of data governance, privacy, and security best practices in clinical research
Competencies
Collaboration: Works effectively with clinical, statistical, and technical teams to align data strategies with study goals
Accountability: Takes ownership of data engineering deliverables and ensures timely, high-quality outputs
Adaptability: Thrives in a fast-paced, evolving environment with shifting priorities and timelines
Compliance-Oriented: Maintains a strong focus on regulatory compliance and data traceability
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Precision Medicine Group is an Equal Opportunity Employer.
Employment decisions are made without regard to race, color, age, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status or other characteristics protected by law.
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📌 Senior Clinical Data Engineer (Latam) (México)
🏢 Precision For Medicine
📍 México