Clinical Research Management Organization conducting Clinical Trials
Our research background, work experience, commitment to delivering high quality results and our large database of patients and PI's (that grows even larger by the day
due to our recruitment procedures and outstanding reputation) give us the benefit of trust that is attracting more and more Sponsors to work directly with us.
Unlike other research facilities, we provide our customer with quality study services such as:
Initial study feasibility
Site recruitment and Accelerated study startup
Centralized management functions
Site Monitoing with Rigorous internal quality control
Motivated, Experienced and dedicated Investigators and study Coordinators
Our main goal is to successfully expedite the approval and marketing of the products held on trial while reducing your costs and maintaining the highest quality standards.
We work effectively with our sponsors to negotiate fair budgets and contracts that lead to win-win relationships and offer the best services to Pharmaceutical and Biotechnology Companies ensuring repeat business opportunities.
By closely working with you and tailoring your needs, we prepare a program that fits both your budget and meets your requirements through the offering of one or more of the following services:
• Study Feasibility Assessment.
• Site Selection.
• Patient Recruitment and Retention.
• Investigator Contracts and Payments.
• Site Monitoring.
• Source Document Preparation and distribution.
• Regulatory Preparation and Submissions.
• Data Management.
• Interactive Voice Response System.
• Clinical Laboratory Services.
• ICH/GCP/CRC Trainings.
• Quality Assurance and Audits.
• Project Management.
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