Sr Clinical Data Scientist

Há 19 horas

Brasília DF, Brasil beBeeClinical Tempo inteiro

Sr Clinical Data Scientist We are seeking an experienced Sr Clinical Data Scientist to fill a key role in our organization. The ideal candidate will have extensive experience in programming for Clinical Data Management Systems (CDMS), 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. Main Responsibilities: Develop, validate, and maintain programming solutions for CDMS, data validation outputs, data review/risk management outputs, custom reports, and programs in clinical trials. Collaborate with data managers, project managers, clinical data scientists, and biostatisticians to ensure the integration of programming solutions into the overall data management process. Act as primary point of contact during study set up and maintenance phase for system programming related questions by the 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 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. Key Skills and Qualifications: Proficiency in programming languages such as SAS, R, or Python. Experience in developing, validating, and maintaining programming solutions for CDMS, data validation outputs, data review/risk management outputs, custom reports, and programs in clinical trials. Strong collaboration and communication skills. Ability to act as primary point of contact during study set up and maintenance phase for system programming related questions. Knowledge of clinical trials environment and concepts of Clinical Data Management Systems. Ability to perform extracts of data from CDMS and creation of data transfer programs. Experience in providing guidance and support to junior programmer levels assigned to a project. Ability to assist in development and implementation of improvements to technical systems and processes within an SME role. Ability to provide guidance on programming best practices, coding standards, and data quality control measures. Ability to stay updated on advancements in programming languages and data management tools to enhance operational efficiencies. Benefits: Opportunity to work with a talented team of professionals. Chance to develop and implement innovative solutions. Professional growth and development opportunities. A dynamic and challenging work environment. Others: This is a full-time position. Must be willing to work in a fast-paced environment.

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