Freelancer profile translated to English.

Description

Experienced CRA, I offer clinical site monitoring, CRF verification, and reporting in compliance with ICH-GCP standards. I am proficient in SOW monitoring, dashboards, and data analysis to ensure the quality and compliance of clinical trials. Available for ad-hoc or regular freelance assignments.

Languages

French
Native or bilingual
English
Fluent
Wolof
Native or bilingual
Bambara
Native or bilingual

Workplace preferences

Remote only

Primarily works remotely

IQVIA
Clinical Research Associate
MEDICAL
June 2025 - Today (1 year)
Clinical Research Associate (CRA) at IQVIA, within the strategic functional partnership (FSP), engaged in conducting quality clinical trials and health innovation.
Clinical Research Oncology Veeva Vault
APHP
Clinical Study Coordinator
MEDICAL
April 2024 - September 2024 (5 months)
Assist investigators in conducting clinical trials through patient screening, inclusion and follow-up assistance, monitoring of serious and non-serious adverse events, data entry, sample handling, protocol adherence, and sponsor contact.
Clinical Research Information verification adherence to procedures
UVSQ
Clinical Study Technician
January 2023 - September 2023 (8 months)
Clinical Study Technician for the Hospital-University Foundation (FHU) Sepsis, based at hospitals: Kremlin-Bicêtre (94); Garches (92), and Ambroise Paré (92).

- Participation in setup meetings with the medical team and the study sponsor
- Participation in the organization of the study in the departments
- Assistance in identifying potential patients (screening)
- Filling out electronic case report forms (CleanWeb, RedCaps) from source documents
- Verification of SAE declarations
Data entry Clinical Research Good practices

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Bachelor of Science in Biology
Sorbonne Université
2022
General Scientific Baccalaureate
Lycée Jean Baptiste Corot
2018

Other

Maïmouna C.

Clinical Research Associate

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