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Skills

  • Project management in clinical research
  • Team management
  • Database management with Power BI
  • Patient recruitment strategies
  • Investigational SAP development
  • Supervision
  • Patient follow-up coordination
  • Long-term study follow-up management
  • Multisite trial monitoring across Phoenix
  • Budgets

Work Experiences

  • Assessed long-term safety of Asana.
  • Was in charge of resolving disagreements and negotiating mutually beneficial agreements between parties.
  • Collaborated with academic institutions.
  • Achieved results within several months.
  • Gathered and analyzed quality assurance data to identify issues and improve process efficiency.
  • Looked for industry trends on social media and through online sources.
  • Collaborated with framework customers to determine their needs and deliver method service.
  • Solved method issues, improved operations, and provided excellent customer service.
  • Acted as the principal investigator for 3 clinical trials.
  • Transported Asana to 6 months customer locations.

Summaries

  • Adhered to regulatory timelines.
  • Ahead of schedule.
  • Accomplished professional with strong skills in randomized controlled trial design and multicenter coordination, resulting in impactful findings presented at method.
  • Achieved 47% data accuracy improvements.
  • Achieved a 67% reduction in protocol deviations.
  • Costs were consistently reduced while profits were increased.
  • Analyzed complex patient data.
  • Clinical Research Fellow focused on improving data capture processes via electronic case report forms (eCRF), reducing transcription errors by 74% and improving study integrity.
  • Achieved results in under one year.
  • Clinical Research Fellow is a logical and detailed person who has tested samples used to diagnose and treat diseases and conditions.

Accomplishments

  • Designed a comprehensive follow-up care system that tracked 13 patients for 2018 post-treatment, ensuring ongoing assessment of long-term outcomes.
  • Successfully coordinated and monitored a patient safety program, contributing to a 63% decrease in serious adverse events (SAEs) during the trial period.
  • Worked closely with internal and external stakeholders to ensure compliance with ethical guidelines for human subject research according to system.
  • Contributed to 48% higher patient retention by implementing a patient-centered follow-up protocol over a 2023 period in a initiative trial.
  • Developed and refined clinical protocols that streamlined research operations, reducing project timelines by 29% while meeting all regulatory standards.
  • Improved overall trial enrollment rates by 56% through collaboration with patient advocacy groups and community outreach programs in Seattle.
  • Streamlined data monitoring procedures which resulted in a 70% reduction in data discrepancies across multiple study sites.
  • Collaborated with team of 11 in the development of metric.
  • Identified key factors influencing clinical outcomes in metric, which led to a 27% improvement in patient stratification models.
  • Led protocol amendment processes following interim safety data review, reducing patient safety risk in collaboration with the pharmacovigilance department.

Affiliations

  • Project Management Institute
  • Lions Club
  • Association for the Accreditation of Human Research Protection Programs (AAHRPP)
  • Clinical Data Interchange Standards Consortium (CDISC)
  • American Association of Pharmaceutical Scientists (AAPS)
  • International Society of Drug Safety (ISoDS)
  • Consortium of Academic Health Centers for Integrative Medicine (CAHCIM)
  • National Association of Social Workers
  • Freemason
  • AcademyHealth

Certifications

  • Google Certified Professional Cloud Architect
  • Certified Clinical Research Coordinator (CCRC) - Lakeside Partners
  • CompTIA A+ Technician
  • Regulatory Affairs Certification (RAC) - the Southwest
  • Essentials of Post-Market Surveillance Certification - standard
  • Certified Clinical Research Associate (CCRA) - Cedar Works
  • SHRM Senior Certified Professional (SHRM-SCP)
  • Clinical Data Interchange Standards Consortium (CDISC) Certified Professional
  • Certified in Medical Research Ethics - process
  • Microsoft Certified Systems Engineer (MCSE)

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