Angel Mayedo
Austin,TX
Summary
Dedicated clinical research coordinator experienced in complying with study protocols, standard operating procedures and good clinical practices. Practiced problem-solver with strong attention to detail. Prepared to offer several years of experience in the field and take on a fast-paced position to make and excellent addition to your team.
Overview
11
11
years of professional experience
Work History
Clinical Research Coordinator
St David's Medical Centre
Austin, TX
05.2017 - Current
- Provided guidance on Good Clinical Practice regulations and other applicable regulatory standards.
- Managed time effectively over 3-5 studies to ensure tasks were completed on schedule and deadlines were met.
- Updated and maintained databases with current and accurate information.
- Demonstrated strong problem-solving skills, resolving issues efficiently and effectively.
- Monitored safety events reported during the course of clinical trials in accordance with SOPs.
- Provided support in writing informed consent forms, patient diaries, study manuals.
- Ensured timely completion of all deliverables by tracking project timelines and milestones.
- Prepared reports summarizing study progress and results for senior management review.
- Tracked enrollment status across multiple studies to ensure target goals were met in a timely manner.
- Analyzed collected data for accuracy prior to database lock; identified discrepancies when necessary.
- Managed blood specimens for clinical trials and processed specimens for sample storage and assay.
Lead Clinical Research Coordinator
Pinnacle clinical Research
Austin, TX
08.2018 - 12.2024
- Oversaw the concurrent management of 6-10 clinical research studies related with Gastroenterology (NASH)
- Performed source document verification, data query resolution and reconciliation of discrepancies.
- Reviewed patient eligibility criteria during screening visits
- Coordinated shipment of investigational product samples to sites.
- Tracked regulatory submissions
- Reviewed protocols, case report forms and other study documents for accuracy.
- Monitored safety events reported by investigators or found during monitoring visits.
- Assisted in the preparation of Institutional Review Board submissions for clinical trials.
- Took vital signs and collected medical histories as part of study protocols.
Medical Assistant, Research Assistant
Austin Area Clinical Trials
Austin, TX
08.2014 - 08.2018
- Familiarized myself with all protocols in order to assist with recruitment processes and cross coverage when needed.
- Worked with physicians and staff to ensure protocol compliance.
- Assisted supervisor/lead coordinators with study start-up including regulatory submission, staff training, education and in-service
- Assisted in ensuring that all queries are resolved in a timely manner in accordance with sponsor requirements.
- Collected data/documents process (completing/collecting sourcedocumentation, CRF completion, AE/SAE reporting, query resolutions, etc.)
- Assisted with maintaining regulatory documents
Lead Certified Medical Assistant
Progressive medical of texas
Austin, TX
01.2014 - 08.2014
- Communicated effectively with other healthcare providers both verbally and through written documentation.
- Answered phone calls from patients seeking advice or assistance with medical issues.
- Greeted patients upon arrival at office visits and verified demographic data before appointment start times.
- Ensured that all patient safety policies were followed throughout each procedure and visit.
- Performed vital signs such as height, weight, blood pressure measurements.
- Collected laboratory specimens according to established protocols.
- Conducted quality assurance checks on all laboratory equipment used for tests or treatments.
Education
CERTIFIED MEDICAL ASSISTANT - Health And Wellness
Everest Institute
Austin, TX12-2013
M.D. - GENERAL MEDICINE
UNIVERSITY OF MEDICINE
HAVANA, CUBA06-2013
Skills
- Investigational product management
- Clinical trial management
- Clinical Data Management
- Informed Consent Process
- Certification in NIH & IATA
- Phlebotomy
- IRB Submissions
- ICH Guidelines
- Case Report Forms
- Quality Control
- Subject Retention Strategies
- Study Start up to Study closures
- Electronic Data Capture
- Research experience
- Good clinical practice
- Time Management
- Task Prioritization
- Bilingual (Spanish)
Affiliations
Spend time with Family in Outdoors
Languages
Spanish
Professional
References
References available upon request.
Timeline
Lead Clinical Research Coordinator
Pinnacle clinical Research
08.2018 - 12.2024
Clinical Research Coordinator
St David's Medical Centre
05.2017 - Current
Medical Assistant, Research Assistant
Austin Area Clinical Trials
08.2014 - 08.2018
Lead Certified Medical Assistant
Progressive medical of texas
01.2014 - 08.2014
CERTIFIED MEDICAL ASSISTANT - Health And Wellness
Everest Institute
M.D. - GENERAL MEDICINE
UNIVERSITY OF MEDICINE