Senior Clinical Programmer Analyst

Há 2 dias

Recife, Brasil Bebeeclinical Tempo inteiro

Job Opportunity:Develop, validate, and maintain programming solutions for clinical trials in the pharmaceutical industry.Key Responsibilities:Collaborate with data managers, project managers, clinical data scientists, and biostatisticians to ensure integration of programming solutions into overall data management process.Act as primary point of contact during study set up and maintenance phase for system programming related questions by project team.Support colleagues with clinical trials environment and concepts of Clinical Data Management Systems.Perform extracts of data from CDMS and creation of data transfer programs.Act as mentor and provides guidance and support to more junior programmer levels assigned to a project.Assist in development and implementation of improvements to technical systems and processes within an SME role.Provide guidance on programming best practices, coding standards, and data quality control measures.Stay updated on advancements in programming languages and data management tools to enhance operational efficiencies.Requirements:Complete bachelor's degree in relevant field such as computer science, SAS, statistics, or life sciences.Extensive experience in programming for CDMS (EDC systems such as Rave/Veeva), data validation outputs, data review/risk management outputs, custom reports, and programs in clinical trials with proficiency in languages such as SAS, R, or Python.Strong problem-solving skills and ability to work collaboratively in fast-paced, cross-functional environment.Excellent attention to detail and organizational skills, with commitment to delivering high-quality results.Strong communication and interpersonal skills, with ability to effectively collaborate with diverse teams and influence outcomes.MUST HAVE advanced English Communication, Writing and Reading

  • Senior Clinical Programmer Analyst

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