When your future rests on the outcome of a study, you need to be swift, nimble, and accurate. Our study start-up is built for that kind of pressure.
Laying the foundation for success
An approach designed to meet your needs
We begin with your goals, listening to your needs – then collaborate to gather and deploy the vital intelligence that gives your trial a solid foundation.
We deliver effective start-up through consistent processes, consistent oversight, and consistent accountability – all tailored to your study’s needs. A study start-up team identifies the sites, compiles the core clinical regulatory package, and supports an effective project launch.
- One dedicated lead oversees every aspect of your global trial, driving timelines, preparing core documents, planning for regulatory processes – and providing one point of contact to address all your questions
- There’s no need for a mirroring structure. Our subject-matter experts handle each key start-up activity, then unify their output in a comprehensive package
- Clear-cut Standard Operating Procedures (SOPs) ensure consistently high quality across deliverables and projects, and our flexible setup prioritizes your study’s unique priorities
PREMIER INSIGHT 242
We knew going in that it could be the perfect recruiting nightmare. We were looking for children ages 2 to 12 for a dermatology study that involved long visits and extensive blood draws.
Getting it right the first time
You get one chance to initiate a clinical trial. Without careful planning, the potential waste of money and time – chronically scarce among biotech and specialty pharma companies – can be devastating.