Manager, Clinical Data Scientist, Clinical Data Sciences
ARG - San Isidro, Argentina
USD 106K-176K (estimate) Mid-level Full Time
Tasks
- Design clinical databases
- Develop data management plan
- Drive data quality and efficiency for data management timelines
- Ensure Trial Master File documentation is filed contemporaneously
- Ensure compliance with SOPs and working practices
- Execute data cleaning and e data processing
- Lead clinical data scientist activities for clinical trials
- Manage data access and visualization
- Manage data acquisition standards
- Oversee data integrity monitoring
- Perform third party study data due diligence
- Release databases
- Select quality risk indicators
- Support study teams with data management standards tools and reporting
- Test and implement CRF and non CRF data collection tools
- Use electronic data capture system for data collection
Perks/Benefits
- N/A
Skills/Tech-stack
Clinical Database | Clinical data | Clinical data management | Clinical database design | Clinical trials | Data Acquisition Standards | Data Capture | Data Integrity | Data Management | Data Management Plan | Data Visualization | Data acquisition | Database Design | EDC | Electronic Data | Electronic data capture | Inform | JReview | MS Access | Master File | MedDRA | Oracle | Oracle RDC | Quality Risk Management | Relational databases | Risk Management | SOP compliance | SQL Server | Spotfire | Trial Master | Trial Master File | WHO Drug
Education
Bachelor of Engineering | Bachelor of Science | Master of Science
Regions
Countries
States
Cities
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