Site Management Services (SMO) - ClinVice

Site Management Services (SMO)

We Offer Tailored Clinical Trial Services

At "ClinVie" Clinical Research Services

Your Trusted Clinical Research Partner in The MENA Region

Site Management Services (SMO)

Site Identification & Feasibility

Site identification & qualification
PI recruitment
Feasibility questionnaire support

Regulatory & Ethics Support

IRB/EC submission preparation
Regulatory document collection
MoH/HA navigation (for each MENA country)

Clinical Trial Start-Up

Contract negotiation support
Site initiation coordination
Investigator meetings
Protocol-specific training
Technique-specific training

CRC Staffing & Oversight

Trained Clinical Research Coordinators
On-site and remote coverage
Backup staffing model

Patient Recruitment & Retention

Site-specific recruitment strategy
Community engagement
Retention materials and logistics

Monitoring Support

Site file readiness
Pre-monitoring visit prep
Query resolution support

Site QA and Audit Preparation

GCP compliance checks
Pre-inspection training
Document QC

Additional Capabilities

Language translation (Arabic-English)
On-site data entry (EDC support)

Optimizing Trial Sites for Speed, Compliance, and Patient Access

We provide Full-Spectrum Operational and Regulatory Support for Clinical Trial Sites, ensuring Rapid Startup, Sustained Enrollment, and GCP-Aligned Execution.

Partner with ClinVice SMO-Submit a Trial Opportunity or call from us.

Discover ClinVice Services Now !

CRO Services

Clinical Research Training Academy

Find Us On

Quick Links

About Us

Services

Partner with Us

Copyright © 2026

Powered by ClinVice