Many clinical research sites, regardless of their location, background, or number of years in the industry, tell us the same thing – new studies are their lifeblood but they don’t have the staff or time to devote to business development.
That’s where CRBD+ steps in. We regularly communicate with major pharmaceutical companies and CROs in the US and beyond as well as with many not-so-well-known sponsors and CROs. Our contacts at these companies are directly involved with site selection and feasibility.
We have over 15 years of experience in contract and budget negotiation, with the last 8 of those specifically in the research field. We also offer a unique perspective, bringing skills from the sponsor, CRO, and site aspects of clinical research.
CRBD+ is more than qualified to handle your business development needs and we are ready to start right now.
Originally from a small town in South Carolina (ask him from where – it’s a great story), Matt started in the medical field right after college. While working in a public health, community-based setting he had his first taste of clinical research where he learned to consent patients enrolling in drug trials. Now, almost 20 years later, he’s held positions in corporate medical research offices, managed sites, and found his niche in business development and consulting. He’s a familiar face at research conferences, certified through ACRP, and sits on one of TransCelerate BioPharma’s site advocacy groups through the Society for Clinical Research Sites.
Today and Tomorrow
At CRBD+, we let our clients show us the way. We are always listening to see how we can assist them, ready to help in any way we can.