Amy Oliver
Saint Louis,MO
Overview
16
16
years of professional experience
Work History
Clinical Research Specialist
Washington University School of Medicine
Saint Louis
08.2020 - Current
- Primary clinical research coordinator for the WeSHARE and WeSHARE Seabird/Sunbird studies
- Supervisor for all other WeSHARE clinical research coordinators and study assistants
- Responsible for all patient safety by meticulously monitoring and documenting all trial related events
- Provided clear guidance to research staff on expectations and responsibilities throughout the study period.
- Trained junior research staff members on proper procedures and protocol adherence, elevating overall team performance.
- Reduced study deviations by implementing strict quality control measures and providing continuous feedback to clinical teams.
- Improved patient enrollment rates by effectively communicating the benefits and risks associated with participating in clinical trials.
- Advanced scientific understanding by co-authoring manuscripts detailing study findings for publication in peer-reviewed journals.
- Streamlined data collection processes for improved accuracy and efficiency in study results analysis.
- Assisted principal investigators in preparing grant proposals, securing funding for critical research projects.
- Increased patient retention rates within studies by fostering strong relationships with participants and addressing their concerns promptly.
- Maximized operational efficiency by developing and maintaining SOPs for various aspects of the clinical research process.
- Promoted a culture of ethical conduct within the research team by stressing the importance of informed consent and adherence to good clinical practice guidelines.
- Supervised data collection by core research staff.
- Designed, constructed and implemented research proposals, protocols and procedures.
- Trained and mentored new staff to achieve efficiency and maintain daily operational consistency.
Clinical Research Coordinator
Washington University School of Medicine
Saint Louis
04.2012 - 03.2016
- Followed clinical research protocols and conducted study visits in compliance with ICH/GCP and FDA regulations.
- Screened patient records, databases, and physician referrals to identify prospective candidates for research studies.
- Gathered, processed, and shipped lab specimens.
- Enhanced patient safety by meticulously monitoring and documenting adverse events during clinical trials.
- Followed informed consent processes and maintained records.
- Collaborated with clinical staff and other healthcare professionals to support clinical trial data accuracy.
- Coordinated and monitored clinical trial activities to support timely and accurate completion of studies.
- Assessed patients'' eligibility criteria following strict adherence to inclusion/exclusion guidelines.
- Maintained compliance with protocols covering patient care and clinical trial operations.
- Developed and maintained accurate and up-to-date case report forms and source documents.
- Reduced data entry errors by implementing stringent quality control measures throughout the study lifecycle.
Clinical Research Coordinator
Washington University School of Medicine
Saint Louis, MO
07.2009 - 04.2012
- Followed clinical research protocols and conducted study visits in compliance with ICH/GCP and FDA regulations.
- Screened patient records, databases, and physician referrals to identify prospective candidates for research studies.
- Gathered, processed, and shipped lab specimens.
- Enhanced patient safety by meticulously monitoring and documenting adverse events during clinical trials.
- Followed informed consent processes and maintained records.
- Collaborated with clinical staff and other healthcare professionals to support clinical trial data accuracy.
- Coordinated and monitored clinical trial activities to support timely and accurate completion of studies.
Education
Master of Social Work - Social Work
Saint Louis University
St. Louis, MO05-2009
Bachelor of Science - Social Work
Saint Louis University
St. Louis, MO05-2007
Skills
- Investigational product management
- Good clinical practices
- Informed consent process
- Electronic data capture
- Adverse event reporting
- Documentation management
- Informed consent
- Clinical trial management
Timeline
Clinical Research Specialist
Washington University School of Medicine
08.2020 - Current
Clinical Research Coordinator
Washington University School of Medicine
04.2012 - 03.2016
Clinical Research Coordinator
Washington University School of Medicine
07.2009 - 04.2012
Master of Social Work - Social Work
Saint Louis University
Bachelor of Science - Social Work
Saint Louis University