Service Overview

Developing a new oncology drug is a complex process requiring sound clinical practices and exacting processes and procedures. Critical to the operation are the experience and expertise of the people conducting the research. Our development teams operate efficiently in a heavily regulated field, managing intricate studies, complex data, ensuring superior study site performance and communication with sites, sponsors and operational staff. We provide a comprehensive selection of clinical research services to pharmaceutical, biotechnology and CRO companies, including: site selection, patient recruitment, project management, site management, clinical trials management, study monitoring and regulatory services, exclusively supporting oncology clinical development. At Oncopartners we thrive in this environment and we welcome you to get to know our staff and to appreciate our commitment to quality research.

Service Offerings

• Study Development Strategy
• Protocol Design
• Feasibility Studies
• Regulatory Review and Submissions
• Investigator Recruitment
• Project Management
• Site Management Services
• Site Support Services
• Patient Recruitment
• Clinical Study Monitoring
• Medical Management / Safety Reporting
• Study Quality Metrics