•Certified Clinical Research Associate.•BS degree in Biology with an emphasis in pharmaceutical science.•Effective communicator; able to manage and coordinate internal and external team activities and collaborate with study management for efficient, timely and accurate data collection and reporting.•Excellent research, document preparation, and record administration skills; including ICF, CRF, and Protocol and SOP development.•Strong organizational skills; ability to prioritize and multitask; self-starter and team player.•Strives for continuous improvement: recognizes inefficiencies in processes and procedures; able to develop and implement innovative solutions. Experienced in Investigator and Site training and re-education on ICH/GCP and study-specifics.•Leadership skills; capable of leading and mentoring study team members and site personnel.•Manages stressful situations in a professional and courteous manner; able to discern escalation to Study Manager.Specialties: CNSEpilepsyPost-operative pain managementGI/Renal Transplantation (lung, liver)DiabetesCardiovascularOncologyMedical DeviceHome office region(s): East Coast (North Carolina) Midwest (Ohio, Illinois)