Randall Liles
Clinical Research Professional
Jacksonville,FL
Summary
CLINICAL RESEARCHER
Passionate patient advocate and highly proficient Clinical Research Professional. Educated, skilled and trained in health science, patient safety, good clinical practices and general trial oversight. Exceptional problem solving capabilities with a team centered approach.
THERAPEUTIC PROFICIENCIES
All phases, I-IV, of pharmaceutical drug trials covering concentrations from vaccines, infectious disease, immunology, endocrinology and metabolic disorders to neurological and cardiovascular medicine. Conducted observational, healthy patient and IMD management studies with pharmaceutical and biotech clients.
Overview
12
12
years of professional experience
Work History
Clinical Research Coordinator
Care Access Research
Jacksonville, FL
12.2021 - Current
- Facilitated quality of clinical trials by establishing project schedules and monitoring support to encourage accuracy and efficiency.
- Collaborated with clinical study site and sponsor to troubleshoot and provide solutions to study-related issues.
- Interfaced with clinical investigators and site staff to foster ethical research consistent with research plans.
- Reviewed clinical data, source documentation, case report forms and investigative site regulatory files to verify accuracy and completion.
- Reviewed data queries and listings and worked with study centers to resolve data discrepancies.
- Implemented electronic data capturing systems to adhere with clinical research guidelines.
Remote Clinical Research Coordinator
WCG- Threewire, Inc
Jacksonville, FL
08.2018 - 07.2021
- Coordinated clinical trials focused on diseases and disorders such as antiviral and antibacterial vaccines, depression, bipolar, obesity and cardiovascular.
- Collaborated with team to define business requirements for organizational processes, achieve productivity and accuracy standards.
- Facilitated direct and remote communication amongst research sites, sponsors and vendors.
- Ensured that all documentation between sites and sponsors was completed accurately, professionally and on time.
- Screened patient records, databases and physician referrals to identify prospective candidates for research studies. Collected data and followed protocols and adhered to standard operating procedures and regulatory reporting requirements.
- Reported all SAE's and AE's to sponsors and regulatory authorities.
- Reviewed all trial documents for IRB and sponsor approval before submitting
- Maintained compliance with ICF and GCP covering patient care and clinical trial operations.
- Generated new business leads through physician referrals, direct patient engagement, deploying outbound marketing tactics and site-optimization.
Public Health Educator
Contractor
Jacksonville , FL
02.2013 - Current
- Conducted clinical events and spoke at health conferences on importance of health education, epidemiology, disease prevention and treatment strategies.
- Led and trained teams of medical professionals in proficient methods and effective delivery of health education.
- Performed health assessments and biometric screenings for various populations throughout southeast region.
- Promoted public health awareness, provided available resources and services to groups and individuals.
- Managed quality assurance program through on-site monitoring, evaluations, internal audits and customer surveys.
Education
Bachelor of Science - Public Health
University of North Florida
Jacksonville, FL12.2012
Skills
- Teamwork
- Attention to Detail
- Good Clinical Practices
- SDR / SDV
- Trial Management and Oversight
- Study Protocols
- ICF Process
- Site-Management and Optimization
- Remote IT Implementation
- Research SOPs
Timeline
Clinical Research Coordinator
Care Access Research
12.2021 - Current
Remote Clinical Research Coordinator
WCG- Threewire, Inc
08.2018 - 07.2021
Public Health Educator
Contractor
02.2013 - Current
Bachelor of Science - Public Health
University of North Florida
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