Senior Clinical Data Engineer – LATAM

🕒 Fevereiro 26

Candidatar-se

Encontrar Vagas Remotas Similares

Configurar Alerta de Email para Novas Vagas

📊 Verifique sua pontuação de currículo para esta vaga

Melhore suas chances de conseguir uma entrevista verificando sua pontuação de currículo antes de se candidatar.

Enviar Currículo

Precision For Medicine

SiteLinkedInTodas as Vagas

1001 - 5000 funcionários

🏥 Saúde

💼 Consultoria

📦 Logística

💰 $75.000.000 Private Equity Round em 2015-12

Healthcare • Consulting • Logistics

A Precision For Medicine é uma organização líder especializada em apoiar o desenvolvimento e a comercialização de terapias inovadoras, particularmente em oncologia, doenças raras e condições autoimunes. Com uma gama abrangente de serviços, incluindo gestão de ensaios clínicos, serviços de laboratório e coleta de biospecimens, eles integram capacidades avançadas de biomarcadores e soluções de manufatura para simplificar os complexos processos de desenvolvimento clínico. Sua missão é acelerar a pesquisa e trazer soluções médicas que mudem a vida dos pacientes, superando as ineficiências tradicionais geralmente encontradas no cenário de desenvolvimento farmacêutico.

Descrição

• Lead the development and optimization of clinical data systems • Drive data standardization and build validation frameworks • Design high-performance databases and pipelines across global trials • Architect scalable validation frameworks to proactively address systemic data issues • Build and maintain modular codebases, set coding standards, and mentor junior engineers • Oversee regulatory alignment with GCP and FDA 21 CFR Part 11 • Develop dynamic dashboards and analytics tools to deliver actionable insights into trial performance and data quality • Act as a strategic liaison across Biostatistics, Clinical Operations, and Regulatory Affairs

🎯 Requisitos

• 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 • Preferred: CRO experience as a Clinical Data Engineer or Programmer

🏖️ Benefícios

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