3-Day Training Workshop
- Daily Duration: 8 hours
- Total Training Hours: 24 hours
- Onsite: Amman, Jordan
Target Audience
- Clinical research coordinators (CRC)
- Clinical research associates (CRA)
- Medical writers
- Research pharmacists
- Investigators involved in clinical trials
- Regulatory affairs professionals
- Clinical research staff at hospitals, universities, government, or CROs
Day 1: Foundations of Clinical Study Protocol Writing
- Focus: Understanding protocol structure and scientific rationale.
- Outcome: Participants learn how to write a clear scientific rationale and background section.
Day 2: Study Design, Statistics, and Protocol Methodology
- Focus: Writing the scientific core of the protocol.
- Outcome: Participants draft key protocol methodology sections.
Day 3 – Quality, Ethics, and Protocol Review
- Focus: Quality assurance, feasibility, and stakeholder collaboration.
- Outcome: Participants complete and review a mini clinical study protocol.
Prerequisite
Participants should have basic knowledge of clinical trials, clinical research concepts, and basic knowledge of clinical trial protocol writing.
Expert-led Training
Dr. Qusai Al-Share Associate Professor of Pharmacology with 17+ years of global clinical research leadership, leading Phase 1–3 trials and contributing to approved therapies.
