Ilias Dahmani
Clinical Data Manager
Experience
Clinical Data Manager
Excelya
- Managed Data Integrity for a Phase IV study (Oncology) leveraging Real-World Evidence (RWE), implementing specialized checks to validate data completeness and ensure regulatory compliance
- Streamlined the Query Resolution Cycle by developing SAS-based tracking and cleaning tools, maintaining high data integrity standards while significantly reducing open query volume to meet delivery timelines
- Targeted review of medical data for interim analyses
- Complete Query Management
Clinical Data Manager
Excelya
- Management of a Phase II clinical trial (pulmonary field) from the setup phase through to intensive data management
- Led and summarized Protocol Deviation and Data Review meetings with cross-functional teams
- Managed data reviews, queries, discrepancy handling, and interim analyses
- Implementation of data review strategies in collaboration with Biostatistics
- Drafted and maintained key documentation: DMP, CMP, eCRF completion guidelines, edit check specs
- Conducted protocol and eCRF review, participated in vendor selection and system validation (EDC & IRT)
- Supervision of the activities of service providers
- Supervised database migrations, freeze and lock, and ensured data compliance with standards
Clinical Data Lead
Sanofi Vaccines
- Contributed to Phase III studies in the vaccine therapeutic area
- Oversaw end-to-end data management: setup, conduct, and close-out
- Designed eCRFs and performed data consistency checks in collaboration with vendors
- Supported database review and protocol deviation management
- Validation of contracts with service providers
Clinical Research Associate (Internship)
Montpellier University Hospital
- Setting up and closing-down remote and on-site studies
- Participation in follow-up visits to various studies
- Submission of substantial modifications to the competent authorities
- Monitoring data on Ennov Clinical
Data Manager (Internship)
INSERM Unit 1058
- Developed reports with R Markdown
- Worked on REDCap setup and report automation for clinical data
Summary
Clinical Data Manager with comprehensive experience across Phase II, III, and IV clinical studies and Real-World Evidence projects in multiple therapeutic areas (oncology, vaccines, and pulmonary diseases). Strong expertise from study setup to database lock, ensuring data integrity, protocol compliance, and adherence to ICH-GCP. Specializing in advanced, risk-based data review via SAS-driven analytics and proactive clinical data management to ensure statistically clean data for critical analysis and rapid database lock. Known for rigorous project follow-up, cross-functional collaboration, and proactive problem-solving.
Skills
Clinical Data Management (Phase Ii, Iii, Iv, Rwe)
Vendor Management
Database Edc Systems: Rave, Viedoc, Veeva, Redcap
Study Setup And Conduct
Protocol Deviations Management
Data Review
Meeting Facilitation
Programming: Sas (Advanced Data Cleaning, Macros, Proc Sql), Sql, R
Protocol Review
Ecrf Review
Irt And Ecrf Uat/at Testing
Data Visualization: Power Bi
Development Of Data Management Plans (Dmp/cmp)
Development Of Edit Check Specifications (Ecs)
Freeze And Lock Management
Database Closure
Risk-based Data Review
Query Management
External Data Reconciliation
Cross-functional Collaboration (Project Managers, Smms, Clinical Scientists, Statisticians)
Microsoft Office
Microsoft Access
Patient, Dynamic, And Reliable
Excellent Communication And Teamwork Skills
Strong Sense Of Responsibility And Commitment To Quality
Languages
Education
Montpellier, Faculty of Pharmacy
Master’s degree · Healthcare Engineering, Clinical Operations & Data Management · Montpellier, France
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