Clinical Research Services
Clinical Research Services help optimize your development timelines, whether your company is developing a biologic, drug or medical device. We offer a range of services to help you achieve your objectives.
We have separate legal entities (staffing, recruiting and CRO). Each helps you solve your problems and remain in compliance during your development.
For example, our Clinical Research Organization helped our client to build a custom team and turn around a study that was receiving poor data from clinical trial sites. The client said we produced the cleanest data and technical writing the Client had ever received. Further, we saved the Client at least $900,000 in labor costs in 1 year according to their measures.
During early-stage development, turn to us to vet and find the best consultants experienced in your therapeutic area. Our expertise is in Clinical, Regulatory and Quality. These consultants will keep you on track with your regulatory submissions. They will ensure your data and product quality support a successful first time FDA approval.
You will also rely on us to plan for the development of your team. We understand the critical inflection points (e.g. preclinical to phase I) when your company will need new talent. We also understand stages at which you will need to seek investor funding, whether through venture capital or an IPO. You can rely on our Executive Search services to dig deep and source candidates to aggressively find the talent your investors want to see.
As your company moves into Phase III and Phase IV, rely on us to serve as your RPO (Recruitment Process Outsourcing).