Detail-oriented Clinical Research Assistant with six years of experience managing various clinical trials at site level. Proficient in study start-up, patient recruitment, data collection, and regulatory documentation. Eager to leverage my expertise and contribute to the success of healthcare innovation.
Overview
6
6
years of professional experience
Work History
Clinical Research Assistant III
DM Clinical Research
Cy-Fair & San Antonio, TX
11.2023 - Current
Compliant with GCP guideline, FDA guidelines, and IRB protocols
Verified, uploaded and filed study documents for CRA review
Roomed patients, took vitals, EKG readings, collected pre-screening medical background
Led initiatives to improve medical record and electronic release of information process to improve retrieval and turnover time of records
Assisted with lab processing and maintained lab documents
Collected post-dose vitals and trained participants on the use of study supplies
Activated and instructed patients on how to utilize an E-diary app to ensure submissions met study compliance requirements
Entered collected data into iMedidata Electronic Data Capture (EDC) system and documented internally in the Clinical Research Information Operations (CRIO) system
Screened patient records, databases, and physician referrals to identify prospective candidates for research studies.
Followed informed consent processes and maintained records.
Collaborated with clinical staff and other healthcare professionals to support clinical trial data accuracy.
Clinical Trial Screening Coordinator
DM Clinical
Cy-Fair, TX
10.2022 - 11.2023
Reviewed vitals, medical history, and current medications
Liaised between recruitment and clinical operations to match subjects with appropriate trials
Educated patients about trial details including schedule of assessments and study investigational products
Coordinated scheduling all follow-up appointments and reminders
Conducted 50 - 100 pre-screening visits to evaluate subject's eligibility
Increased efficiency within the department by regularly reviewing workflow processes and making adjustments as needed.
Patient Enrollment Specialist
DM Clinical
Houston, TX
06.2020 - 10.2022
Surpassed daily scheduling targets and exceeded outgoing call quotas to support enrollment objectives
Reviewed and analyzed protocols to ensure alignment with inclusion and exclusion criteria
Engaged with diverse populations to volunteer as participants in research studies
Collaborated with marketing team to promote an ambassador program
Clinical Site Intern
DM Clinical
Tomball, TX
06.2019 - 08.2019
Assisted with clinical data management and study coordinators
Contributed to a ground-breaking Continuous Glucose Monitoring study for the Dexcom device
Facilitated site study inventory management and ensured timely study e-diary compliance
Supported staff members in their daily tasks, reducing workload burden and allowing for increased focus on higher-priority assignments.
Gained valuable experience working within a specific industry, applying learned concepts directly into relevant work situations.
Sorted and organized files, spreadsheets, and reports.
Gained hands-on experience in various software programs, increasing proficiency and expanding technical skill set.
Clinical Assistant III - Medsurge/Telemetry Monitor Technician at Brackenridge HospitalClinical Assistant III - Medsurge/Telemetry Monitor Technician at Brackenridge Hospital
Advanced Medical Support Assistant (Clinical Research Hub) at U.S. Department of Veterans Affairs – VA Palo Alto Health Care SystemAdvanced Medical Support Assistant (Clinical Research Hub) at U.S. Department of Veterans Affairs – VA Palo Alto Health Care System