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Mariem RahoMR

Mariem Raho

Clinical Research Consultant/CRA/Project Manager

€650/day
Paris 14e Arrondissement, FR
8-15 years

Average response time: 1 hour

Freelancer profile translated to English.
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About Mariem

Specialist in late-stage, I support my clients in the implementation of their Phase III - IV clinical studies / RWE studies, post-CE marking clinical investigations for medical devices in France, academic studies, and this, at all stages of execution (initiation, startup, execution, monitoring/oversight, closure).
More than 15 years of experience in Clinical Research.
Passionate about Clinical Research, I created Clin4all, an agile CRO aimed at facilitating the implementation of clinical studies in France. Our services:
- Project management,
- Medical writing,
- Regulatory submissions
- Study startup,
- Site contract management,
- Monitoring, CRA roles
- Investigator support, CTA roles
- Data analysis
- Valorization
- Data management and statistical analysis (via our partners).
Do not hesitate to contact me to discuss your projects.
See you soon!
  • French

    Native or bilingual

  • English

    Fluent

Can work on-site
Paris 14e Arrondissement (up to 50km)

Experience

  • Clin4all CRO
    Clinical Research Consultant
    MEDICAL
    June 2020 - Today (6 years)
    Île-de-France, France
    1/ Freelance assignments for various pharmaceutical companies, medical device manufacturers, medtech, and international CROs:
    - Clinical Project Manager
    - Regulatory Affairs Manager / Contract Specialist
    - Senior CRA
    - Data Entry Specialist
    2/ Operations Management / Team Management within the CRO Clin4all
    3/ Quality Assurance Manager at CRO Clin4all
    4/ Business Management at CRO Clin4all
    Clinical research Project management Monitoring medical device Clinical Trials
  • CPP IDF VIII
    Ethics Committee Evaluator
    MEDICAL
    November 2018 - June 2021 (2 years and 8 months)
    Paris, France
    Review and evaluation of applications for research involving human subjects in terms of scientific, methodological, ethical, and regulatory aspects:
    - Phase I, II, III, IV trials
    - Clinical investigations on medical devices
    - Care research
    - Observational studies/cohorts
  • CESP - Centre de recherche en Epidémiologie et Santé des Populations
    Scientific Project Manager
    MEDICAL
    September 2018 - June 2021 (2 years and 10 months)
    Région de Paris, France
    Scientific and operational coordination of studies in the field of HIV
    Project management
    Co-creation of eCRF
    Document writing
    Implementation of Risk-based monitoring, performance monitoring, data review
    Digital Communication Correspondent for the department

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Education

  • Master 2 Public Health: Methodology and Biostatistics in Biomedical Research (M2)
    Paris Sud University (Paris XI)
    2016
  • Engineering degree in Life Sciences
    National Conservatory of Arts and Crafts
    2015
    Titre du mémoire: Les déterminants sociaux de santé des personnes vivant avec le VIH : une approche par le score EPICES (score individuel de vulnérabilité sociale)

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