Freelancer profile translated to English.
Back to original languageAbout Adama
Clinical research consultant specializing in structuring, coordination, and data management.
Consultant with over 4 years of experience, I support CROs, sponsors, and research centers in the implementation, management, and structuring of their clinical research activities.
I am primarily involved in:
- Coordination and operational monitoring of clinical studies
- Structuring of research processes and organization
- Data management (collection, quality control, eCRF and query management)
- Monitoring and follow-up of investigator sites
- Document management (TMF/eTMF)
- Contribution to regulatory activities (submissions, file tracking)
- Budget monitoring of sites and payment management
My goal: to ensure data quality, regulatory compliance (GCP), and adherence to deadlines.
Autonomous, rigorous, and quickly operational, I easily integrate into project teams and adapt to study needs.
Mainly available for remote work, with the possibility of on-site intervention depending on project needs.
French
Native or bilingual
English
Fluent
Spanish
Basic
Can work on-site
Paris (up to 50km)
Experience
- Institut de Cancérologie du Centre (ICC)Clinical Research Consultant – Structuring & CoordinationMEDICALJune 2026 - TodaySaint-Doulchard, FranceOngoing mission within an oncology clinical research center, as part of the development and structuring of research activities.Involvement in:- Structuring and organization of clinical research activities- Coordination and implementation of clinical trials- Development of partnerships with academic and industrial sponsors- Implementation of management tools (indicators, dashboards, monitoring)- Contribution to the launch and follow-up of initial trialsRegulated environment – collaboration with medical teams and external partners.
- Registre MucoviscidoseClinical Research Consultant – Data Management & MonitoringMEDICALApril 2026 - Today (2 months)Paris, FranceRecent mission for collecting and managing clinical data for a national registry.- Collection and entry of clinical data- Quality control and inconsistency management- Processing of patient records (DPI)- Coordination with hospital teams- Compliance with quality and confidentiality requirements
- Vaincre La MucoviscidoseCoordination and operational monitoring of a national clinical registryMEDICALSeptember 2022 - May 2025 (2 years and 8 months)13th arrondissement, 75013 Paris, FranceManagement of the French national cystic fibrosis registry. Coordination with hospitals, conducting training sessions on eCRF.Organization of site visits and management of relationships with clinical teams. Participation in major collaborative projects (Kaftrio, Ciment, Modul CF). Management of queries and regular exchanges with clinical teams. Creation and updating of eCRFs to optimize data collection.
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Education
- Data Analyst TrainingCulture Data & IA2025Formation Data Analyste
- DIU Health Training for Clinical Research AssociatesUniversité Claude Bernard Lyon 12022DIU Santé Formation des Attachés de Recherche Clinique
Certifications
- ICH E6 (R2) Good Clinical PracticeThe Global Health Network2024
Skill set
Categories
- Other