Accomplished Clinical Research Associate with 7 years' experience in performing and documenting pre-study site evaluations, site initiations, regulatory document collection, interim monitoring and study close-out visits. Diligent in performing studies in accordance with good clinical practices, study-specific requirements, clinical monitoring plans, company procedures, applicable regulatory requirements and defined quality standards. Clear communicator when working with internal teammates and external contacts. Hardworking Senior Clinical Research Associate adept at leading site evaluations, initiations and closeouts. Well-versed in outdoors trials and capable of picking up new procedures quickly. Offering advanced planning, problem-solving and communication skills developed over 3+ years in the field. Seasoned Professor with 12 years in higher education. Committed to public education and community service. Seeking challenging role as clinical research associate.