We are a full-service CRO with a focus in oncology. Having a therapeutic concentration promotes refinement of our expertise, skills and tools throughout the organization. Our team is energized by the complexities and challenges of the ever-changing landscape that defines oncology research.
Our CPMs offer diverse and broad skill sets – essential traits for meeting the needs of small biotech companies
Clinical Study Monitoring
Our team of CRAs are adept in managing the nuances of oncology trials
Our Medical Monitor and Clinical Scientist roles work in tandem to support the clinical needs of the study
Our cross-functional team approach to data review allows clients to make timely data-driven decisions
“Excellence” is in our name and is what we strive for.
From IND submission to CSR, we can support your medical writing needs
Our validated platform allows for a streamlined approach to collect, manage, analyze, and report safety events
A simplified technology solution to manage, track, and report all activities associated with your clinical trial
We provide the expertise needed when preparing clinical data across studies for a regulatory submission
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(We also provide ballpark costs for your clinical development planning)