Detail-oriented Clinical Research Coordinator with proven expertise in patient recruitment, adverse event reporting, data management and regulatory compliance. Committed to upholding good clinical practices and enhancing trial efficiency.
Overview
1
1
Certification
8
8
years of professional experience
Work History
Clinical Research Coordinator
Spokane Urology
Spokane
07.2024 - Current
Coordinated patient recruitment and retention efforts for clinical trials.
Managed data collection and maintained accurate records in compliance with regulatory standards.
Assisted in developing study protocols and informed consent documents for research projects.
Collaborated with investigators to ensure adherence to study timelines and objectives.
Monitored adverse events and reported findings to regulatory bodies as required.
Facilitated communication between patients, clinicians, and sponsors to enhance study efficiency.
Followed clinical research protocols and conducted study visits in compliance with ICH/GCP and FDA regulations.
Prepared and maintained regulatory documents for clinical trial submissions.
Monitored unit budget to meet financial objectives for spend rate and funding.
Clinical Research Coordinator
Memorial Sloan Kettering/Eight Eleven Group
New York, NY
02.2023 - 02.2025
Enhanced patient safety by meticulously monitoring and documenting adverse events during clinical trials.
Collaborated with clinical staff and other healthcare professionals to support clinical trial data accuracy.
Reduced data entry errors by implementing stringent quality control measures throughout the study lifecycle.
Developed strong relationships with trial sponsors, ensuring ongoing collaboration and future project opportunities.
Emergency Medical Technician
Accucare Medical Group
St Louis, MO
12.2020 - 03.2023
Responded promptly to emergency calls, providing critical care and support during transport.
Administered basic life support techniques, ensuring patient safety and comfort.
Collaborated with healthcare professionals to develop effective treatment plans in high-pressure situations.
Conducted thorough assessments of patients' conditions, documenting vital signs and medical history accurately.
Streamlined communication processes between dispatch and field teams to improve response times.
Evaluated incident reports for accuracy, implementing changes to enhance operational efficiency and safety standards.
Enhanced patient care by efficiently assessing and addressing medical emergencies in high-pressure situations.
Clinical Research Coordinator
The University of Kansas Cancer Center
Mission, KS
03.2022 - 02.2023
Screened patient records, databases, and physician referrals to identify prospective candidates for research studies.
Gathered, processed, and shipped lab specimens.
Followed informed consent processes and maintained records.
Coordinated and monitored clinical trial activities to support timely and accurate completion of studies.
Worked with principal investigator and sponsors to facilitate daily trial activities and comply with research protocols.
Facilitated clear communication between principal investigators, sponsors, and study participants for seamless trial execution.
EKG Technician
The University of Kansas Medical Center
Kansas City, KS
08.2018 - 11.2020
Conducted EKG tests adhering to established protocols and safety standards.
Monitored patient vital signs during procedures to ensure safety and accuracy.
Collaborated with healthcare team to interpret results for effective treatment plans.
Trained new staff on operational procedures and equipment usage for optimal performance.
Managed EKG equipment maintenance, ensuring readiness for clinical use at all times.
Developed best practices that improved workflow efficiency in cardiac testing processes.
Led quality assurance initiatives, enhancing accuracy of diagnostic results significantly.