Freelancer profile translated to English.
Back to original languageAbout Dignê
Doctor of Health Sciences with solid expertise in clinical research (phases I to IV), protocol development, and scientific communication. I am experienced in conducting multicenter clinical trials, budgeting, and managing registries in the fields of oncology, rare diseases, cardiovascular and metabolic pathologies. I can contribute to study design, clinical data analysis, and the development of clinical development strategies, providing robust scientific insights to inform decision-making and improve patient care.
French
Native or bilingual
English
Native or bilingual
Arabic
Basic
Spanish
Basic
Can work on-site
Paris (up to 50km)
Experience
- IQVIAClinical Research CoordinatorMEDICALMarch 2026 - Today (5 months)Dijon, France• Contribute to the scientific supervision of oncology clinical trials, ensuring protocol adherence and data integrity.• Participate in the review and interpretation of clinical data to support evidence generation and medical decision-making.• Collaborate with investigators and cross-functional teams, facilitating scientific exchange and alignment around study objectives.• Participate in patient recruitment strategies and contribute to study feasibility and implementation.
- CHU LIMOGESSenior Clinical Research AssociateMEDICALOctober 2025 - April 2026 (6 months)Limoges, France• Responsible for coordinating and optimizing imaging and radiology services integrated into all clinical studies conducted within the institution:
- Close scientific collaboration with clinicians, researchers, and the Research and Innovation department,
- Clinical trial setup, logistical organization, patient follow-up, and collaboration with multidisciplinary medical teams (oncology, cardiology, geriatrics, gynecology, hematology, etc.),
- Research support: participation in patient identification, inclusion, and randomization, eCRF, Queries.
- Contribution to protocol review, feasibility assessment, and clinical trial implementation.
• Monitoring of adverse events/serious adverse events, regulatory archiving, inspection preparation, and continuous process improvement.• Participation in cross-functional medical activities, such as preparing scientific meetings, disseminating medical information,• Interaction with internal and external stakeholders (researchers, sponsors, CROs) to ensure the scientific quality and regulatory compliance of clinical data. - Assistance Publique des Hôpitaux de ParisClinical Research AssociatePUBLIC SECTOROctober 2023 - October 2025 (2 years)Paris, France• Participate in protocol review, report clinical assessments, and ensure clinical trial implementation.• Take part in cross-functional medical activities, such as participating in scientific meetings.• Ensure the scientific quality and regulatory compliance of clinical studies.• Respond to grant applications for research study funding.• Setup, logistical organization, and patient consent processes.
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Education
- Doctor of Health Sciences (PhD)University of Reims Champagne Ardenne2023Grade: Félicitations du jury (rapport de la soutenance ci-joint) ; 27,5/20 ECTS Activities and societies: *European Atherosclerosis Society (EAS); *Nouvelle société francophone d’Athérosclérose (NSFA); *Société Française de la Biologie de la Matrice ExtraCellulaire (SFBMec). Au cours de ma formation pratique doctorale j’ai travaillé sur l’identification et la caractérisation fonctionnelle de nouveaux partenaires d'interaction d'une sialidase membranaire (neuraminidase-1, NEU-1) dans les macrophages humains. A ce jour, mes travaux sur trois ans et malgré l'impact de l'épidémie de la crise COVID19, ont donné lieu à 03 publications scientifique, 09 communications (orales et affichées ) lors de congrès internationaux et nationaux et 02 prix de valorisations. Par ailleurs, j'ai eu à compléter ma formation par l'enseignement supérieur et en validant 27,5 / 20 crédits ECTS de l'école doctorale via 09 modules en plus d'un Diplôme Universitaire notamment : *Matrice extracellulaire; *Ma thèse en 180 secondes - Challenge international de médiation scientifique; *Techniques de communication; *Management des Hommes; *Gestion des conflits; *Gestion de projet; *DU en Expérimentation Animale (niveau 3/3). Skills: Cardiovascular Disease, Life Sciences, +7 skills
- Master 2: Pathophysiology of Epithelia and CancersUniversité Paris Cité2019Ce parcours développe les bases fondamentales cellulaires et moléculaires régissant l’organisation et les fonctions des tissus épithéliaux, en étroite connexion avec les aspects cliniques. Les épithéliums tapissent l’ensemble des cavités de notre organisme et délimitent l’intérieur de l’extérieur. Identifier les facteurs qui contrôlent l’acquisition, le maintien et l’adaptation du phénotype épithélial, comprendre les mécanismes impliqués dans les pathologies innées ou acquises et en trouver les traitements appropriés, constituent aujourd’hui un des grands défis de la recherche biomédicale. Skills: Oncology, Life Sciences, +3 skills
Certifications
- Clinical Project ManagerDe Vinci Education2025
- Medical Science Liaison (MSL) / Regional Medical Representative (RMR)Université Paris Cité2024
Skill set
Categories
- Other