We’ll Guide You Every Step of the Way.

To get your product to market as efficiently as possible, we offer comprehensive clinical trial services, from protocol design to FDA submission. Our team of medical, regulatory, operational and statistical oncology experts design and execute your program to ensure its utmost success. With a passion for excellence, our staff provides the same level of commitment to each step of study execution, including state-of-the-art communications and project management, cutting-edge data management systems and processes, and expert data analysis and summarization from our oncology statisticians and medical writers.

Our comprehensive Oncology Services include:

Program and Study Design
- Clinical Development Planning
- Strategic Regulatory Consulting
- Protocol Design
Rapid Study Start-up
- Site and Investigator Identification and Feasibility Assessments
- Site Budgets, Contracts and Payments
- Investigator Meeting Planning and Coordination
- Patient Recruitment Strategies
Trial Management
- Program and Clinical Trial Management
- Clinical Monitoring
- Medical Monitoring
- Pharmacovigilance
Data Collection and Reporting
- Data Management
- EDC platforms featuring technology transfers of Phase Forward InForm™ and Medidata Rave™
- Oracle Clinical system for paper-based trials
- Biostatistics
- Medical Writing

Over the past year, we have fortified our oncology capabilities through the acquisition of Prologue Research and the oncology operations of OSI Pharma. The result is the formation of a business unit focused on the unique demands of oncology studies. Together, our new oncology business unit offers a full range of clinical research services for Phase I-IV international or US-based clinical trials in oncology and oncology-related studies.

We’re proud to be focused on making a meaningful difference in the lives of people with cancer.