Clinical Research Coordinator

Profile: Certified Clinical Research Associate professional with extensive recent focus in CVS research and clinical trials. Combine resourcefulness and problem solving skills with clinical knowledge to consistently deliver improved research and production results. Team player dedicated to quality, continuous improvement and bottom-line objectives. QUALIFICATION HIGHLIGHTS • Knowledgeable in all areas of research including budgeting, ICH/GCP, IRB protocol submissions, on-going regulatory and IRB phases and IND safety reporting. • Demonstrated competencies in managing clinical trials data, formulating source documents and data collection charts and severe adverse event reporting. • Proven project management abilities with capacity to design, plan and implement ideas from conception through completion; able to manage multiple responsibilities without compromise to detail or quality. • Outstanding interpersonal skills; equally comfortable communicating one-on-one or addressing large audiences. Solid ability to translate technical information to staff, physicians and patients. • Committed to quality patient care; frequently recognized by physicians for strict attention to detail, patient advocacy and decision-making abilities in critical situations.

Clinical Research

Phoenix, AZ