Versatile clinical research professional knowledgeable about coordinating patient information, laboratory samples and compliance documents for diverse clinical trials. Highly organized and thorough with good planning and problem-solving abilities. Well-versed in study protocols, standard operating procedures and general trial oversight. Track record of being an essential part of any leadership team or executive role and is highly instrumental in providing effective solutions that immediately creates an impact, contributing to the company’s forward moving success. Ready to bring my professional experience to a challenging new role.