Candidate Information Name Available: Register for Free Title Clinical Research Coordinator Target Location US-TX-Amarillo Email Available with paid plan Phone Available with paid plan	20,000+ Fresh Resumes Monthly     View Phone Numbers     Receive Resume E-mail Alerts     Post Jobs Free     Link your Free Jobs Page     ... and much more Register on Jobvertise Free
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Street Address  Redwood StAmarillo Texas Street Address
EMAIL AVAILABLEPHONE NUMBER AVAILABLELINKEDIN LINK AVAILABLEHighly motivated and detail-oriented Clinical Research Coordinator with over 2 years of experience in conducting and managing clinical trials. Proven track record in regulatory compliance, data management, and patient recruitment. Skilled in coordinating teams, ensuring adherence to protocols, and contributing to scientific publications.Medical AssistantMedical AssistantVista College, Amarillo, TexasGraduation Year: 2013Business Administration BBAStrayer UniversityGraduation Year: June 2026**Certifications**- Good Clinical Practice (GCP) Certification, 2022**Professional Experience****Clinical Research Coordinator**Amarillo Center for Clinical Research Amarillo, TxMay 2022  Present- Manage and monitor clinical trials ensuring compliance with regulatory requirements and study protocols.- Coordinate site initiation, interim monitoring, and close-out visits.- Develop and review informed consent forms and case report forms.- Train and support site staff on study procedures and protocols.- Perform source document verification and ensure data accuracy and integrity.- Assist in the preparation and submission of regulatory documents to IRBs/ECs.- Coordinated patient recruitment, enrollment, and follow-up for multiple clinical trials.- Maintained accurate and timely documentation in electronic data capture (EDC) systems.- Conducted patient assessments and managed adverse event reporting.- Communicated with sponsors, CROs, and regulatory authorities to ensure study compliance.- Prepared and submitted regulatory documents and progress reports.**Skills****Clinical Trial Management:** Protocol development, site monitoring, patient recruitment**Regulatory Compliance:** GCP, FDA, IRB/IEC submissions**Data Management:** EDC systems, data entry, source document verification**Communication:** Patient communication, report writing, stakeholder collaboration**Awards and Honors**- PHI THETA KAPPA Honor Society, 2023- The National Society of Collegiate Scholars, 2023**References**Available upon request.