Ahmad Shtaiwi

Business Development at International Pharmaceutical Research Center (IPRC)
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Contact Information
us****@****om
(386) 825-5501
Location
Jordan, JO
Languages
  • Arabic -
  • English -

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Credentials

  • Linear Regression in R for Public Health (Coursera - Imperial College London)
    Coursera
    Dec, 2020
    - Nov, 2024
  • Logistic Regression in R for Public Health (Coursera-Imperial College London)
    Coursera
    Dec, 2020
    - Nov, 2024
  • Statistics in Medicine, Statement of Accomplishment from Stanford University. Online based course
    Stanford University
    Jul, 2018
    - Nov, 2024
  • Project Management Professional (PMP)
    Project Management Institute
    Jun, 2017
    - Nov, 2024

Experience

    • Business Development
      • Dec 2021 - Present

  • Freelance
    • Amman, Jordan
    • Clinical Research Consultant
      • Jun 2020 - Present

      Consulting service for different aspects in the clinical research including: • Designing and writing clinical trials protocols • Writing statistical analysis plan and performing statistical analysis for clinical trials using various softwares (SPSS, SAS, STATA) • Responding to the regulatory authorities’ queries and questions regarding clinical trials files submission. • Training clinical trial team on writing clinical trial study protocols and analysing study results. Consulting service for different aspects in the clinical research including: • Designing and writing clinical trials protocols • Writing statistical analysis plan and performing statistical analysis for clinical trials using various softwares (SPSS, SAS, STATA) • Responding to the regulatory authorities’ queries and questions regarding clinical trials files submission. • Training clinical trial team on writing clinical trial study protocols and analysing study results.

    • Jordan
    • Pharmaceutical Manufacturing
    • 1 - 100 Employee
    • Head of Data Management
      • Jan 2020 - Jun 2020

      • Performing statistical & pharmacokinetic analysis and interpreting the bioequivalence trials results using different software, like: SAS, STATA & WinNonlin • Designing clinical trials particularly bioequivalence studies • Supervising trial protocols and reports writing • Ensuring trial’s compliance with Good Clinical Practice (GCP) principles • Performing statistical & pharmacokinetic analysis and interpreting the bioequivalence trials results using different software, like: SAS, STATA & WinNonlin • Designing clinical trials particularly bioequivalence studies • Supervising trial protocols and reports writing • Ensuring trial’s compliance with Good Clinical Practice (GCP) principles

    • Regulatory, Biometric and Medical Affairs Manager
      • Mar 2015 - Sep 2018

      • Designing clinical trials particularly bioequivalence studies • Supervising trial protocol writing • Ensuring trial’s compliance with Good Clinical Practice (GCP) principles. • Following up trial approvals with the local authority and ethics committee, and responding to their queries • Direct communication with external sponsors and responding to issues related to trial conduction progress and results • Creating timelines for various projects and making the arrangements to make sure that the all deadlines are fulfilled assuring the completeness and accuracy of the job. • Participating in budgeting of clinical trials • Performing pharmacokinetic analysis and interpreting the bioequivalence trials results using WinNonlin • Supervising writing of the trial final reports Show less

    • Jordan
    • Hospitals and Health Care
    • 700 & Above Employee
    • Clinical Research Coordinator
      • Dec 2012 - Feb 2015

      • Organizing, facilitating and coordinating clinical trials particularly phase II and III clinical trials. • Ensuring compliance with local and international regulations for human subject research and clinical trials. • Following and implementing in-house policies and procedures for clinical trial conduct. • Reviewing and providing commentary to clinical trial agreements. • Organizing, facilitating and coordinating clinical trials particularly phase II and III clinical trials. • Ensuring compliance with local and international regulations for human subject research and clinical trials. • Following and implementing in-house policies and procedures for clinical trial conduct. • Reviewing and providing commentary to clinical trial agreements.

    • Jordan
    • Pharmaceutical Manufacturing
    • 200 - 300 Employee
    • Medical representative
      • Feb 2009 - Nov 2011

      • Organising appointments and meetings with community- and hospital-based healthcare staff • Presenting products to healthcare staff including doctors, nurses and pharmacists • Attending and organising trade exhibitions, conferences and meetings • Reviewing sales performance • Participated in setting the sales target plan • Worked on a study of pricing change and its effect on drugs sales. • Organising appointments and meetings with community- and hospital-based healthcare staff • Presenting products to healthcare staff including doctors, nurses and pharmacists • Attending and organising trade exhibitions, conferences and meetings • Reviewing sales performance • Participated in setting the sales target plan • Worked on a study of pricing change and its effect on drugs sales.

  • al-hayat pharmaceutical company
    • Amman Governorate, Jordan
    • Medical Representative
      • Sep 2007 - Feb 2009

Education

  • University of York
    MSc Applied Health Research, Health Science
    2018 - 2019
  • Al-Jami'ah Al-Urdunia
    M.Sc., Pharmaceutical Sciences
    2010 - 2014
  • Al-Jami'ah Al-Urdunia
    BS, Pharmacy
    2001 - 2006

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