MBA, CEO and Founder
Trinh brings over 30 years of broad operational experience in all aspects of the biotechnology/pharmaceuticals and CRO industry specializing in early clinical development. Her natural leadership skills and ability to remove obstacles and move projects forward combined with her hands-on approach to all aspects of clinical trials has helped her establish a truly collaborative team who has a can-do attitude.
Chief Operating Officer
Daniel has over 30 years of experience in GxP environments serving in both the military and biotech/pharmaceutical industry. His unique experience in project management, clinical supplies chain management, quality systems and engineering (I&C, metrology/facility systems) allow for leveraging the skills and experience to deliver high-quality clinical research solutions for CCRC’s clients.
RN, VP of Operations
Deidre draws on her more than 30 years of drug development (CRO and pharma) and nursing experience in early clinical development to provide oversight, guidance, and implementation strategies to ensure all projects are conducted with an emphasis on subject safety and client satisfaction while adhering ICH and GCP guidelines. Her focus is on specialized rapid study start up and subject recruitment strategies as well as timeline and budget adherence.
CCRC builds lasting relationships with our clients, medical professionals and third-party vendors resulting in a vast network of connections which we leverage to meet the needs of your clinical trials.
CCRC has collaborated with CROs of all sizes, domestic and international.
We work towards building lasting relationships with our clients, medical professionals and third party vendors. By coming together in unison we can achieve more. Contact us to learn how we can collaborate together.