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Marwa LotmaniML

Marwa Lotmani

Clinical Research Associate | eCRF & Clinical Data

€200/day
Paris, FR
0-2 years

Average response time: 1 hour

Freelancer profile translated to English.
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About Marwa

Holder of aMaster 2 in Biochemistry and Immunologyand certifiedClinical Research Associate (CRA)**, I apply my scientific rigor and my mastery of **Good Clinical Practices (GCP)to your research projects.

Thanks to my background in biology, I work on clinical study projects, ensuring the quality, consistency, and reliability of the data.

My key skills:

**Data Management & eCRF**: Entry, verification, and quality control of clinical data with a compliance-oriented approach.


Regulatory Documentation**: Management and updating of the **Trial Master File (TMF)and protocol monitoring.



**Medical Data Entry**: Rigor and respect for patient data confidentiality.


I am recognized for my rigor, my attention to detail, and my ability to work autonomously.

📍 Available for freelance missions (remote or hybrid)
  • French

    Native or bilingual

  • English

    Fluent

Can work on-site
Paris (up to 30km)

Experience

  • Formatis
    Junior Clinical Research Associate (CRA)
    MEDICAL
    November 2025 - December 2025 (1 month)
    Vélizy-Villacoublay, France
    **Certified Clinical Research Associate (CRA) GCP / ICH-GCP**, I combine solid expertise in clinical biochemistry with specialized training in clinical trial monitoring. With experience in a hospital setting at the CHU of Oran, I am proficient in data management (CRF/eCRF), Trial Master File (TMF) maintenance, and rigorous quality control of protocols. My dual scientific (Master 2) and regulatory profile allows me to ensure the compliance and reliability of clinical data with great autonomy.
    eCRF TMF Monitoring Good Clinical Practice Oncology
  • LABORATOIR CENTRAL BIOCHIMIE «
    Study Engineer in Clinical Biochemistry
    September 2022 - December 2023 (1 year and 3 months)
    Laboratoire centrale du CHU, Oran, Algeria
    • Perform biochemical analyses on biological samples, following established protocols and quality standards.
    • Interpret analysis results and issue precise and reliable reports within deadlines.
    • Maintain and calibrate laboratory equipment used for biochemical analyses to ensure their accuracy and reliability.
    • Participate in the evaluation and validation of new biochemical analysis methods, in collaboration with the research and development team.
    • Supervise daily laboratory activities, including staff training and resource management.
  • CHU DR BENZERDJEB
    Biochemical Analyses
    May 2021 - October 2021 (5 months)
    Orán, SA, Argentina
    • Perform collection and preparation of biological samples for analysis.
    • Use laboratory equipment to perform biochemical tests.
    • Analyze experimental data and interpret results.
    • Follow experimental protocols and implement procedures.
    • Participate in the validation of analysis methods. Equipment maintenance and calibration. Documentation of experiments and results.
    • Adhere to laboratory safety and ethical standards.

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Education

  • Clinical Research Associate (ARC E-TECH)
    Formatis MultiHealth
    2025
    Attaché De Recherche Clinique (ARC E-TECH)
  • Master 2 Degree
    University of Oran-1 Ahmed Ben bella
    2022
    Diplôme Master 2

Skill set

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