Senior Clinical Data Engineer – LATAM

🕒 February 26

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Precision Medicine Group

WebsiteLinkedInAll Job Openings

1001 - 5000 employees

Founded 2012

🧬 Biotechnology

⚕️ Healthcare Insurance

💊 Pharmaceuticals

💰 $35.2M Venture Round on 2021-03

Biotechnology • Healthcare Insurance • Pharmaceuticals

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 • Drive data standardization initiatives • Build validation frameworks and design high-performance databases and pipelines across global trials • Serve as a strategic partner to Clinical Data Managers and cross-functional teams • Lead compliance initiatives to ensure all data systems and workflows meet GCP, FDA 21 CFR Part 11, and evolving global regulatory requirements • Develop and operationalize dynamic dashboards and analytics tools that provide real-time insights into data quality, trial progress, and operational KPIs • Act as a strategic liaison between Clinical Data Engineering and other departments

🎯 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 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

🏖️ Benefits

• Health insurance • Paid time off • Flexible work arrangements • Professional development