Danny Kakish

Background

About Danny Kakish

I am a highly skilled Senior Clinical Research Coordinator with nearly two decades of experience in the industry. Throughout my career, I have developed a deep understanding of ALCO and (ICH) GCP standards and have applied them to Phase II-IV clinical trails in both IRO and Decentralized Clinical Trials. I have worked in therapeutic areas including Family Medicine, Pediatrics, Cardiology, Gastroenterology, Mental Health, Women's Health, Psychiatric, Orthopedic, and Rheumatology. My expertise includes managing studies from startup to closeout, overseeing site operations, managing budgets and contracts, phlebotomy and lab, ensuring regulatory compliance and reporting, EDC entry and compliance, recruitment, managing enrollment, and retention efforts. I have worked extensively with SMOs, CROs, and the FDA. I have a proven track record of delivering high-quality results in both IRO and DCT settings. My strong attention to detail, excellent communication skills, and ability to work effectively with cross-functional teams make me an ideal candidate for any clinical research role. ACRP member, SOCRA member, GCP certified, IATA certified, BBS certified, and BLS certified.