Ahmad Shtaiwi
Business Development at International Pharmaceutical Research Center (IPRC)- Claim this Profile
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Arabic -
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English -
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Bio
Credentials
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Linear Regression in R for Public Health (Coursera - Imperial College London)
CourseraDec, 2020- Nov, 2024 -
Logistic Regression in R for Public Health (Coursera-Imperial College London)
CourseraDec, 2020- Nov, 2024 -
Statistics in Medicine, Statement of Accomplishment from Stanford University. Online based course
Stanford UniversityJul, 2018- Nov, 2024 -
Project Management Professional (PMP)
Project Management InstituteJun, 2017- Nov, 2024
Experience
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International Pharmaceutical Research Center (IPRC)
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Jordan
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Research
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1 - 100 Employee
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Business Development
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Dec 2021 - Present
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Freelance
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Amman, Jordan
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Clinical Research Consultant
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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.
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ACDIMA BioCenter
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Jordan
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Pharmaceutical Manufacturing
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1 - 100 Employee
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Head of Data Management
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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
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PRU (Pharmaceutical Research Unit)
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Amman_ Jordan
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Regulatory, Biometric and Medical Affairs Manager
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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
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King Hussein Cancer Foundation and Center
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Jordan
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Hospitals and Health Care
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700 & Above Employee
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Clinical Research Coordinator
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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.
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Joswe Medical
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Jordan
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Pharmaceutical Manufacturing
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200 - 300 Employee
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Medical representative
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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.
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al-hayat pharmaceutical company
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Amman Governorate, Jordan
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Medical Representative
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Sep 2007 - Feb 2009
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Education
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University of York
MSc Applied Health Research, Health Science -
Al-Jami'ah Al-Urdunia
M.Sc., Pharmaceutical Sciences -
Al-Jami'ah Al-Urdunia
BS, Pharmacy