Brenda Vasquez Email and Phone Number

Managed patient recruitment, informed consent process and data entry to support trial objectives. Review and comprehend active study protocols and utilize multiple platforms for managing patient data and scheduling.

Develop QC checklists, trackers and other QC tools designed to track the QC review process. Ensure all QC data is complete and entered in appropriate platforms within the required time frame. Maintained compliance with protocols covering patient care and clinical trial operations, ensuring protection of all participants.

• Properly documenting EMR, ensuring a seamless workflow for the physician and quality care of the patient• Accountable for documentation that supports billing, coding and critical care levels• Contributed to ensuring compliance with discharges, admission, and transfer processing, as well as Sepsis, Stroke and Code Heart protocols.• Accompanied physicians through day in fast-paced, stressful environments.• Charted patient encounters by recording information such as diagnosis, treatments, and prescriptions, and selected appropriate ICD-10 and CPT codes for records.• Interacted with physicians, nursing staff, technicians and medical assistants throughout facility.• Stayed on top of current patient loads to facilitate efficient and organized workflow.• Developed advanced proficiency in electronic medical records management software.• Reviewed records, paperwork, and orders for errors and resolved issues with minimal direction.• Followed all HIPAA rules and regulations regarding patient confidentiality.

Worked with principal investigator and sponsors to facilitate daily trial activities and comply with research protocols. Maintained compliance with protocols covering patient care and clinical trial operations. Followed informed consent processes and maintained records. Screened patient records, databases, and physician referrals to identify prospective candidates for research studies. Collected data and followed research protocols, operations manuals, and case report form requirements. Assist in project planning and implementation. Monitored patient safety throughout clinical trials and reported any adverse events. Followed clinical research protocols and conducted study visits in compliance with ICH/GCP and FDA regulations. Coordinated and monitored clinical trial activities to support timely and accurate completion of studies.