Title: Data Scientist
Location: Remote
Duration 4-6 months
Job Summary- Data Scientist (RBQM - Clinical Trials)
- Support central monitoring and risk-based quality management (RBQM) for clinical trials.
- Implement and maintain pre-defined KRIs QTLs and risk metrics using robust SAS programming.
- Extract transform and integrate clinical data from EDC systems (e.g. RAVE) into analysis-ready SAS datasets.
- Generate routine and ad-hoc RBQM/central monitoring outputs (tables listings data extracts dashboard feeds).
- Perform quality control and troubleshooting of SAS code to ensure accurate and efficient outputs.
- Maintain comprehensive technical documentation for all RBQM programs and processes.
- Collaborate with cross-functional teams (Central Monitors Data Management Biostatistics Study Operations) to understand requirements and ensure correct implementation of RBQM metrics.
- Utilize advanced SAS programming skills and work with large complex clinical trial datasets.
- Preferred experience with RAVE EDC CDISC standards and data visualization tools.
- Applies strong clinical development and data science expertise to support robust and scalable analytics across multiple clinical studies.
Title: Data Scientist Location: Remote Duration 4-6 months Job Summary- Data Scientist (RBQM - Clinical Trials) - Support central monitoring and risk-based quality management (RBQM) for clinical trials. - Implement and maintain pre-defined KRIs QTLs and risk metrics using robust SAS programming....
Title: Data Scientist
Location: Remote
Duration 4-6 months
Job Summary- Data Scientist (RBQM - Clinical Trials)
- Support central monitoring and risk-based quality management (RBQM) for clinical trials.
- Implement and maintain pre-defined KRIs QTLs and risk metrics using robust SAS programming.
- Extract transform and integrate clinical data from EDC systems (e.g. RAVE) into analysis-ready SAS datasets.
- Generate routine and ad-hoc RBQM/central monitoring outputs (tables listings data extracts dashboard feeds).
- Perform quality control and troubleshooting of SAS code to ensure accurate and efficient outputs.
- Maintain comprehensive technical documentation for all RBQM programs and processes.
- Collaborate with cross-functional teams (Central Monitors Data Management Biostatistics Study Operations) to understand requirements and ensure correct implementation of RBQM metrics.
- Utilize advanced SAS programming skills and work with large complex clinical trial datasets.
- Preferred experience with RAVE EDC CDISC standards and data visualization tools.
- Applies strong clinical development and data science expertise to support robust and scalable analytics across multiple clinical studies.
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