Beatriz Medina, ND

• Worked with principal investigator and sponsors to facilitate 250 monthly safety follow-ups for large scale respiratory study
• Demonstrated timely and efficient query resolution
• Performed study visits that included vital signs, ECG, and phlebotomy.
• Worked directly with remote CRAs and study personnel to perform Adverse event follow-ups
• Performed Medical record reviews with PI for timely SAE reporting
• Maintained compliance with protocols covering patient care and clinical trial operations.
• Collected data and followed research protocols, operations manuals and case report form requirements.
• Screened patient records, databases, and physician referrals to identify prospective candidates for research studies.
• Followed informed consent processes and maintained records in accordance with Standard Operating Procedures
• Proved successful working within tight deadlines and fast-paced atmosphere for light speed clinical trials
• Gathered, processed and shipped lab specimens.

• Maintained participant compliance with protocols via daily emails, and responding to participant inquiries remotely
• Provided participant study support., trial education, and guidance remotely
• Created and provide weekly participant compliance summary reports to study team and sponsor.
• Completed and Audited CRFs for large (4,500 enrollees) de-centralized respiratory study
• Developed and improved study participant compliance report using Excel , and EDC systems.
• Exceeded goals through effective task prioritization and great work ethic.

• Coordinated clinical trials focused on respiratory disorders.
• Worked with principal investigator and sponsors to facilitate daily trial activities and comply with research protocols.
• Collected data and followed research protocols, operations manuals and case report form requirements.
• Completed daily and weekly Safety review visits for over 300 participants in vaccine clinical trial
• Documented and reported Adverse Events to study site and PI
• Performed medical record reviews for SAE reporting

• Screened patient records, and databases to identify prospective candidates for research studies.
• Actively recruited and enrolled participants
• Worked with principal investigator and sponsors to facilitate daily trial activities and comply with research protocols.
• Performed input, retrieval, and analysis of data for processing and validation.
• Followed informed consent processes and maintained records.
• Maintained compliance with protocols covering patient care and clinical trial operations.
• Maintained data management systems for multiple studies
• Demonstrated strong writing skills to generate original correspondence and reports.
• Performed spectroscopic analysis of human lab specimens
• Handled all troubleshooting tasks on malfunctioning lab equipment working with manufacturers to resolve problems.

• Assisted COVID lab team with skilled analyses by preparing COVID samples for Q-PCR testing.
• Performed high volume pipetting of 400-500 samples per day
• Evaluated quality control within laboratory using standard laboratory test and measurement controls.
• Analyzed bodily fluids with laboratory equipment and detected anomalies related to diseased states.
• Retrieved results from computer records when requested by physicians and other healthcare workers, and, when necessary, directed inquiries to appropriate laboratory staff
• Maintained strict aseptic fields when collecting biological samples to minimize infection risks.
• Participated in continuing education and learning experiences to enhance and maintain current knowledge and skills.
• Used Microsoft Excel and other software tools to create documents and other communications.
• Used critical thinking to break down problems, evaluate solutions and make decisions.

• Supported instructor with test administration, curriculum development and assignment grading for Homeopathy III
• Guided students through using homeopathic software (MacRepertory)
• Tutored 35 students in classical homeopathy principles, case taking, and posology.
• Supported student learning objectives through personalized and small group assistance.

• Trained and assisted new hires with laboratory specimen protocols and processing

• Assisted in developing and managing new hire training manual

• Provided resolutions for daily questionable lab specimens to inpatient and offsite nursing staff

• Processed and packaged research participant specimens for shipping according to research protocols

• Contacted physicians, nursing stations or reference laboratories for resolution assistance with unusual test orders.
• Maintained documentation on tests performed in lab.
• Performed testing and quality control using approved laboratory procedures and instrumentation.