General Inquiries
We build a trust-based relationship with each site, ensuring the right level of oversight and providing support to study personnel throughout all stages of the clinical study. We firsthand understand the daily challenges that study personnel encounter as they juggle clinical research alongside their regular clinical duties. That's why we aim to streamline their work whenever possible and offer support in every way we can.
Site Management Services
Identifying the appropriate clinical sites, conducting Site Initiation Visits (SIV), selecting Principal Investigators (PI), recruiting patients, and finalizing necessary contract agreements with these stakeholders.
Reporting serious adverse events to the Sponsor or CRO and the Institutional Review Board/Independent Ethics Committee (IRB/IEC).
Advicing and alerting investigators about potential protocol violations.
Submission to Institutional Review Board/Independent Ethics Committee (IRB/IEC) for approval.
Submission to the Jordan Food and Drug Administration (JFDA) for approval.
Comprehensive Site Selection and Project Management Services
Appointment of Clinical Research Associates (cCRAs)
Counseling and Recruitment of Patients
Patient Follow-up
Translation of Informed Consent Forms (ICF)
Site Initiation, Activation, and Trial Close-Out Operations
Archiving and Maintenance of Trial-Related Documents
Ensuring Compliance with the Protocol
Advising and alerting investigators about potential protocol violations.
Advising and alerting investigators about potential ICH-GCP compliance issues.
Clinical Trial Site Management
ClinicalTrialsUA - Your Assurance for Effective Site Management
Effective site management is paramount for the seamless execution of clinical trials. At ClinicalTrialsUA, we guarantee this critical component, offering a range of services to ensure trials operate smoothly and in compliance with regulations. Our expertise covers coordinating activities, from participant recruitment to meticulous data collection and strict adherence to ethical and regulatory standards.
Our careful site management prioritizes the safety of all involved parties, ensuring not only the quality and accuracy of data but also the well-being of trial participants
Interested in receiving a proposal from ClinicalTrialsUA? How you choose to get in touch depends on your query type
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For CRO & Sponsors
Interested in ClinicalTrialsUA SMO's network, principal investigators, and capabilities?
For investigators | PI | Sites
We are looking for physicians, clinics, health systems or other research organizations that want to develop a strategic partnership offering clinical research as a care option for patients.
For patients
Patient care is at the heart of everything we do, and we are committed to ensuring you are treated with the utmost care and respect whilst maintaining the highest standard of research.
