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Mehdi Saad, PhD

Mehdi Saad, PhD

Internship

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  • Timeline

  • About me

    Medical Affairs Manager, Interventional Cardiology - EMEA

  • Education

    • Université de Caen Normandie

      2016 - 2016
      Diplôme Universitaire Clinical Data Management

    • Université Paris-Saclay

      2013 - 2017
      Doctor of Philosophy - PhD Public Health

      Early detection and objective quantification by chronoamperometric measurement of peripheral neurologic impairment in patients receiving neurotoxic chemotherapy

    • Université de Versailles Saint-Quentin-en-Yvelines

      2012 - 2013
      Master's degree Clinical study coordination (Coordinateur d'études dans le domaine de la santé)

    • Université Denis Diderot (Paris VII)

      2010 - 2012
      Master's degree Biochemistry and Molecular Biology

    • Université de Versailles Saint-Quentin-en-Yvelines

      2008 - 2010
      Bachelor's degree Biology

  • Experience

    • Tunis Design

      Jul 2008 - Jul 2008
      Internship

      Bioinformatics / Data Processing

    • SANOFI-AVENTIS

      Jul 2010 - Jul 2010
      Internship

      Galenic development of generic drugs:- Follow-up of the production chain- Performing chemical and microbiological tests.

    • Institut du Cerveau et de la moelle épinière (ICM)

      Jan 2012 - Jun 2012
      Internship

      Postnatal electroporation as a model for studying oligodendrocyte generation:- Standardization of a technique: post-natal electroporation in mice.- Overexpression of a transcription factor involved in the generation of oligodendrocytes and study its degree of involvement in the differentiation of neural stem cells into oligodendrocytes.- Presentation of preliminary results at the ARSEP congress (ARSEP Foundation for Research on Multiple Sclerosis)

    • Hôpital de la pitié salpêtrière

      Sept 2012 - Sept 2013
      Clinical Research Associate

      - Follow-up of 2 trials involving the study two treatments in association or not with radiotherapy in patients with high-grade cerebral tumour. - Writing and submitting applications for the labelling of a referral centre for the management of patients suffering from neurological complications due to anti-cancer treatment.

    • Impeto Medical SAS

      Sept 2013 - Dec 2016
      Clinical Project Manager

      Clinical Project Manager - Medical Device:- Writing of study documents (protocol, consents, etc ...)- Regulatory submissions (amendments, authorizations requests, etc ...)- Site selection, follow-up of recruitments and organization of site visits- Data management and statistical analysis - Scientific Writing (abstracts and scientific articles for submission to peer review journals)- Participation in national and international conferences/congresses.

    • SAS Allocations & Conseils

      Jan 2017 - Mar 2017
      Trainee

      Data management in financial markets:- Participation in the development and implementation of the data base of an investmentfund selection software- Training in the distribution of insurance products/contracts

    • RaDiCo, French National Program on Rare Disease Cohorts

      May 2017 - Mar 2018
      Clinical Project Manager

      - Management of European clinical studies- Study documents writing (Protocol, Case Report Forms)- Technical and regulatory instruction for clinical studies- Supervision and management of Clinical Research Associates - Budget and timelines set-up

    • European Drug Development Hub (EDDH)

      Apr 2018 - Jan 2019
      International Clinical Project Manager

      - Management of european clinical trials (Phase II clinical trials)- Management of service providers and contracotrs- Oversight of monitoring activities + co-monitoring (UK) when needed.- Regulatory submissions (Ethic Committees & Competent Authorities)- Study documents writing (Protocol, case report forms, reports)

    • Kantar Health

      Jan 2019 - Apr 2019
      International Clinical Project Manager

      - Project planning, scheduling and implementation- Optimize resources allocation- Management of project budget and financial performance- Coordination of the different functional units involved in the projects (Data Management, Statistics, Pharmacovigilance & Regulatory)- Study documents writing (Protocol, case report forms)

    • B. Braun Groupe

      May 2019 - Sept 2021
      Global Clinical Project Manager

      - Management of international clinical studies (Interventional & non-interventional studies)- Management of Real World Evidence/Real World Data studies- Internal & External data dissemination

    • Boston Scientific

      Sept 2021 - now
      Medical Affairs Manager, Interventional Cardiology - EMEA

      - Collaborated with EMEA marketing groups and Global Scientific Affairs to plan and develop high-quality physician medical and scientific content at 3rd party congresses or Boston Scientific sponsored events.- Proactively engaged with identified Healthcare Professionals (HCPs) and Key Opinion Leaders (KOLs) to exchange clinical data, exploring clinical areas of need, and aligning with corporate initiatives.- Evaluated external clinical research proposals and collaborated with the HEMA and EMEA marketing groups to advise on how research proposals fit the overall evidence generation strategy. Show less

  • Licenses & Certifications

    • Good clinical Practice

      Formedea
      Nov 2018