Ricardo Thompson
@ricardothompson
I am a global clinical research leader delivering compliant, on-time, on-budget trials.
What I'm looking for
I am a results-driven clinical research leader with 15+ years directing global trials and optimizing study operations. I have led cross-functional teams across multiple countries, created detailed project plans, and developed risk mitigation strategies to prevent delays.
I have improved patient recruitment and retention, maintained audit-ready documentation with zero major findings, and supervised teams of up to 15 staff while ensuring SOP and GCP adherence. I hold a Master of Science in Public Health and a Bachelor of Science in Biology, and I focus on delivering quality outcomes within budget and regulatory guidelines.
Experience
Work history, roles, and key accomplishments
Senior Project Manager
ICON Clinical Research
Oct 2021 - Apr 2025 (3 years 6 months)
Directed multiple global clinical projects, aligning scope, resources, and timelines with sponsor expectations and meeting all contractual and regulatory requirements. Coordinated cross-functional teams across 7 countries and executed risk mitigation strategies to prevent delays while maintaining strong stakeholder relationships.
Clinical Site Director
Global Medical Research Institute
Feb 2017 - Oct 2021 (4 years 8 months)
Led daily operations for multiple concurrent Phase I–IV trials, supervising and mentoring up to 15 research staff and improving compliance and team performance. Conducted feasibility assessments that accelerated study start-up timelines and increased patient recruitment through targeted community outreach.
Clinical Research Manager
Delray Medical Center
Jan 2016 - Jan 2017 (1 year)
Created and implemented research workflows to improve operational efficiency and ensured audit readiness and regulatory compliance across all studies. Streamlined trial documentation and coordinated interdisciplinary teams to meet study deadlines and quality standards.
Senior Research Coordinator
Premiere Research Institute
Nov 2011 - Jan 2016 (4 years 2 months)
Managed screening, evaluation, and testing for study subjects and supported protocol submissions, amendments, and renewals while maintaining audit-ready regulatory binders. Collaborated with principal investigators to ensure protocol adherence and patient safety across neurological and cardiology studies.
Clinical Research Associate
Northwest Regional Hospital
Liaised with investigators to ensure accurate trial data collection and adherence to protocols, supporting monitoring and source data verification activities. Maintained study documentation and contributed to audit readiness.
Clinical Research Supervisor
Northwest Regional Hospital
Directed protocol design, trial monitoring, and data management oversight to ensure accurate and compliant study conduct. Supervised research staff and enforced SOPs to maintain data integrity and regulatory readiness.
Epidemiologist
Office of Epidemiology
Investigated disease outbreaks and developed prevention strategies, conducting statistical analyses to inform public health improvement programs. Implemented interventions that supported community health monitoring and response efforts.
Education
Degrees, certifications, and relevant coursework
Nova Southeastern University
Master of Science, Public Health
Completed a Master of Science in Public Health at Nova Southeastern University in Fort Lauderdale, FL.
Nova Southeastern University
Bachelor of Science, Biology
Earned a Bachelor of Science in Biology from Nova Southeastern University in Fort Lauderdale, FL.
Tech stack
Software and tools used professionally
Availability
Location
Authorized to work in
Job categories
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