
1001 - 5000 employees
🏥 Healthcare
💼 Consulting
📦 Logistics
💰 $75M Private Equity Round on 2015-12
Healthcare • Consulting • Logistics
Precision For Medicine is a leading organization that specializes in supporting the development and commercialization of innovative therapies, particularly in oncology, rare diseases, and autoimmune conditions. With a comprehensive range of services including clinical trial management, lab services, and biospecimen collection, they integrate advanced biomarker capabilities and manufacturing solutions to streamline the complex clinical development processes. Their mission is to accelerate research and bring life-changing medical solutions to patients by overcoming traditional inefficiencies typically found in the pharmaceutical development landscape.
🔥 14 minutes ago
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1001 - 5000 employees
🏥 Healthcare
💼 Consulting
📦 Logistics
💰 $75M Private Equity Round on 2015-12
Healthcare • Consulting • Logistics
Precision For Medicine is a leading organization that specializes in supporting the development and commercialization of innovative therapies, particularly in oncology, rare diseases, and autoimmune conditions. With a comprehensive range of services including clinical trial management, lab services, and biospecimen collection, they integrate advanced biomarker capabilities and manufacturing solutions to streamline the complex clinical development processes. Their mission is to accelerate research and bring life-changing medical solutions to patients by overcoming traditional inefficiencies typically found in the pharmaceutical development landscape.
• Lead the development and optimization of clinical data systems across global trials • Drive enterprise-level data standardization and mapping initiatives • 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 • Ensure compliance with 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 data quality, trial progress, and operational KPIs • Translate complex datasets into actionable insights for clinical and regulatory stakeholders • Liaise with Biostatistics, Clinical Operations, and Regulatory Affairs • Translate clinical and scientific requirements into scalable technical solutions • Design and optimize secure, high-performance relational databases and data lakes • Build and maintain ETL pipelines integrating data from diverse clinical systems
• 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 experience • Dashboard development experience • CDISC governance knowledge • 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 • Ability to extract pertinent information from protocols, electronic study data systems and clinical systems • Proficiency in statistical analysis and data monitoring tools • Strong analytical and problem-solving skills • Experience with integrated risk planning and management • Ability to mentor junior team members • 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
• Remote work arrangement • Equal Opportunity Employer • Reasonable accommodation for applicants with disabilities
Apply Now🔥 14 minutes ago
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