À propos de Manal
Healthcare professional with clinical nursing experience and exposure to medical devices in hospital environments (ICU, operating rooms, inpatient care).
I support clinical research and healthcare projects through coordination, communication, documentation, and operational assistance. My clinical background allows me to understand study environments from both a patient care and operational perspective, helping bridge communication between healthcare teams and research or project stakeholders.
I am particularly interested in clinical research operations, healthcare project coordination, and patient-centered studies.
Core areas of support:
- Clinical study coordination and follow-up support
- Patient communication and participant support
- Study logistics (scheduling, tracking, coordination of activities)
- Clinical documentation and data entry support
- Literature review and research assistance
- Cross-functional communication between clinical, research, and operational teams
- Administrative support for healthcare and clinical projects
Background:
- Clinical nursing experience (ICU, OR, inpatient care)
- Hands-on use of medical devices in real hospital settings
- Exposure to healthcare systems and public health concepts
- Academic foundation in epidemiology and health economics
I am detail-oriented, reliable, and motivated to contribute to structured clinical and healthcare projects while continuing to build experience in clinical research operations.
Arabe
Bilingue ou natif
Anglais
Capacité professionnelle complète
Français
Capacité professionnelle complète
Accepte de travailler sur site
Paris (jusqu’à 20 km)
Expériences
- PROMAMECRegulatory Affairs Trainee – EU MDR Implementation and export projectmars 2023 - août 2023 (5 mois)
- Supported regulatory documentation alignment for Class IIa and IIb medical device procedure kits in preparation for EU MDR compliance and CE-marking processes targeting European market access.
- Worked on technical documentation updates for single-use surgical kits composed of imported and locally manufactured components, ensuring documentation consistency across product descriptions, labeling, applicable regulations, standards, and supplier-related information.
- Reviewed and organized regulatory documentation including risk, performance, and technical data to improve file completeness and facilitate alignment with EU MDR requirements.
- Collaborated with regulatory, technical, and cross-functional teams to maintain updated documentation and support progress of CE-marking preparation activities.
- Contributed to the development and documentation review of 7 surgical procedure kits, integrating both regulatory requirements and end-user clinical considerations based on healthcare workflow knowledge.
- CHU de BesançonClinical Investigation Intern – Medical Devices – Pre-CE MarkSECTEUR MÉDICALnovembre 2022 - janvier 2023 (2 mois)Besançon, France
- Contributed to development of a Clinical Investigation Plan (CIP) for a Class II medical device intended for home-use adaptation.
- Supported study design development including endpoints, patient eligibility criteria, follow-up schedules, and outcome measures.
- Contributed to clinical documentation aligned with EU MDR and ISO 14155 requirements for CE-marking preparation.
- Reviewed prior clinical studies, PMCF data, and safety/performance evidence to support clinical strategy.
- Ministère de la Santé marocaineAnesthesia and Intensive Care NurseSECTEUR MÉDICALjuin 2020 - août 2021 (1 an et 2 mois)Morocco
- Worked in high-pressure hospital environments during the COVID-19 pandemic, managing care delivery in isolation units with complex and rapidly evolving protocols.
- Faced with critical patient flow challenges and infection control constraints, I coordinated daily operations alongside multidisciplinary teams including physicians, military medical staff, and civilian nurses. I acted as a team support lead within a group of healthcare professionals, ensuring continuity of care and effective communication across stakeholders.
- Provided direct patient care in ICU and inpatient settings, ensuring adherence to clinical protocols, patient safety, and quality standards under high-risk conditions.
- Supported clinical decision-making and operational coordination for patient transfers to higher-level care units (including intensive care and emergency services), in collaboration with attending physicians.
- Contributed to clinical education by informing patients and families about disease conditions, isolation protocols, and treatment pathways, improving understanding and adherence to care procedures.
- Trained nursing students on the use of medical devices and supported proper application in clinical settings, contributing to risk reduction and procedural compliance.
- Participated in laboratory-related processes including biological sample collection, labeling, documentation, and handling, ensuring accuracy and traceability of clinical data.
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Formations
- Master of Science, Technology, Health – International Master in Biomedical EngineeringInstitut Supérieur d’Ingénieurs de Franche-Comté (ISIFC)2023Master 2
- International Master’s Degree in Biomedical EngineeringAbulcasis International University of Health Sciences - UIASS2022Master 1
Certifications
- Essentials of European Medical Device Regulations (EU MDR)-2017/745Alison2023
- ISO 13485:2016 - Quality Management Systems for Medical DevicesAlison2022
Compétences
Catégories
- Autre