Associate Director, TMF Operations and Clinical Operations Analytics
Philadelphia, Pennsylvania, United States
USD 137K-190K (estimate) Senior-level Contract Full Time
Tasks
- Assess analytics and reporting systems
- Communicate performance metrics to stakeholders
- Create reporting metrics and KPIs
- Develop TMF metrics and KPIs
- Develop TMF standards and SOPs
- Ensure inspection readiness
- Ensure reporting solutions are fit for purpose
- Govern TMF vendor committees
- Implement TMF support model
- Interpret analytics and drive insights
- Lead clinical operations reporting and analytics strategy
- Manage TMF vendors
- Manage data mapping for reporting
- Negotiate TMF budgets
- Oversee TMF operations
- Review TMF input for clinical documents
- Serve as TMF systems representative
- Support regulatory audits
Perks/Benefits
- N/A
Skills/Tech-stack
Adobe Acrobat | Analytics | Audit Readiness | CDISC Trial Master File Reference Model | CDMS | CTMS | Clinical Trial Master File | Clinical trial | Data Mapping | Document Management | EDC | EDMS | Electronic TMF | ICH GCP | KPI Development | Master File | Microsoft Excel | Microsoft PowerPoint | Microsoft Project | Microsoft SharePoint | Microsoft Word | Reference Model | Regulatory Compliance | Reporting | Risk Management | SOP Development | Trial Master File | Trial Master File Reference Model | Veeva | Veeva Vault | Veeva applications | Vendor management
Education
Roles
Regions
Countries
States
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