Associate Data Manager, Clinical Data Sciences
USA - NY - Headquarters, United States
USD 68K-114K Mid-level Full Time
Tasks
- Apply clinical data standards
- Conduct e data processing
- Document testing and validation
- Ensure SOP compliance
- Execute quality database design
- File TMF documents contemporaneously
- Generate DM metrics reporting
- Implement clinical data collection tools
- Maintain Trial Master File documents
- Manage clinical data review
- Manage data access and visualization
- Manage data queries
- Perform data cleaning
- Release database for submission readiness
- Support CRF and non CRF data collection
Perks/Benefits
- 401k
- Caregiver leave
- Dental coverage
- Health benefits
- Medical leave
- Paid Holidays
- Paid vacation
- Parental leave
- Personal days
- Prescription Drug Coverage
- Vision coverage
Skills/Tech-stack
CRF | Clinical data | Clinical data management | Data Capture | Data Management | Data Processing | Data Query | Data Testing | Data Validation | Data Visualization | Data access | Data cleaning | Data query management | Database Design | EDC | Electronic Data | Electronic data capture | Electronic filing | FDA Regulations | J Review | Master File | MedDRA | Microsoft Excel | Microsoft Outlook | Microsoft Word | Non CRF | Query management | SOP compliance | Spotfire | TMF | Trial Master | Trial Master File | WHO Drug
Education
Roles
Regions
Countries
States
Cities
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