Integrating Into Your Trial Process Easier and Getting You to Decision Points Faster.
As a mid-sized CRO, we consider ourselves to be the “right size” outsourcing partner. While we are small enough to provide you with a personal touch and keep the focus where it belongs—on you, with a global reach across 32 countries, in all the key drug development markets, we are also big enough to conduct large and complex global trials and support your larger IIb and III studies.
Consider the advantages:
Strong Therapeutic Experience History. We see a tremendous demand for very specialized, complex therapeutic expertise across all service areas. Our therapeutic bandwidth enables us to understand the challenges of treating complicated diseases that allow us to service your trial needs in a customized manner.
Global/Program Efficiencies. Utilizing global best practices for all of our drug development programs creates program efficiencies, where we have an ongoing application of lessons learned. This can create a tremendous cost savings both now and later.
Project Acceleration. We can help get your product to market faster through our key ‘fast-track’ offerings like our KickStart® dedicated database building team and our SmartStartSM project kick-off planning process.
Site Management And Patient RecruitmenT (SMART) Team. We strive to better understand your patients and their needs. The SMART team leverages effective patient recruitment and strategic site relationships to facilitate successful trial enrollment. We target the right patients from the very beginning through optimal site identification, and then focus on how to get your patients the greatest level of benefit for treating their disease.
Proven Governance Model. Our Executive Leadership believes in being not only visible, but accessible to both you and the project teams. Close metrics management, prompt issue escalation and action planning, and a strong overall relationship oversight are all key to our strategy.
Highly Qualified and Experienced PDs. Most of our Project Directors are PMP certified, and our experts provide a road map for successful trial management from inception to close and beyond.
Global Footprint. Our global footprint extends from Latin America to Asia Pacific and North America to Europe, so we are able to provide a location close to you. This enables us to be regional experts, which can translate to large cost benefits for your large programs. We help assess the right strategy for your particular trial and maximize cost savings in the process.