Qualification Highly motivated and accomplished Clinical Research Coordinator with extensive skills and experience. Nine years of experience as an Oncology research coordinator. Proven ability to manage multiple studies simultaneously. Managed phase 1b - IV protocols according to GCP and FDA guidelines. Experience as a supervisor and mentor to study coordinators across various oncology disease sites. Trained staff on study protocol, procedures, pharmacokinetics, CRF completion, SAE reporting, and auditing. Seeking a long -term, permanent position in a clinical and / or scientific environment allocating proficient, analytical, problem solving skills. Bilingual: Fluent in Spanish. CCRP certified.

Highlights:

• Appraisals
• Audit
• Clinical Research
• Data Quality
• Documentation
• Management
• Protocol
• Quality
• Quality Assurance
• Recruiting