- Our Project Management service is critical to ensure that trials are set up, enrolled, conducted, and reported on-time and on-budget.
- Our experienced PMs are responsible for the study throughout the clinical trial life cycle, starting from its planning, implementation and finalization.
- At MENA Clinical Research, we assure fast site readiness and preparation for site initiation. Our experienced CRAs will be responsible for
performing site training (initiation visit) to the investigative site and will assure site readiness for patient recruitment.
- Our CRAs will be responsible for site monitoring including On-site visits (IMV) and Remote Monitoring Visits (RMV).
- Our CRAs are managing the sites by performing continuous trainings and risk management, our aim is to provide our clients with high quality data.
- We at MENA Clinical Research are dedicated to performing ongoing trainings for our CRAs including annual GCP training as well as ongoing trainings on the site monitoring activities, local regulations, and company SOPs. We perform trainings to assure that our CRAs are up to date receiving their continuous training.
- In addition to site monitoring visits, and due to the continuous need of the remote environment, our monitoring strategies support the remote monitoring calls and visits that can be done based on client decision and approval to support sites and keep continuous follow up with them.