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Skills

  • Business operations
  • Automated data entry system implementation
  • Clinical quality assurance
  • Cohort demographics analysis
  • Informed consent
  • Multi-site study management
  • First Aid/CPR
  • Good Clinical Practices
  • Good Clinical Practice (GCP) adherence
  • Standard equipment

Work Experiences

  • Gathered, analyzed, and modeled the data.
  • Achieved 19% faster data entry.
  • Aligned projects with study sponsor expectations.
  • Solved procedure issues, improved operations, and provided excellent customer service.
  • Collaborated with process customers to determine their needs and deliver category service.
  • Conducted comprehensive training.
  • Coordinated multiple clinical trials.
  • Clinical trials for disorders like category and standard were coordinated by me.
  • Had an excellent attendance record and was always on time for work.
  • Achieved goals within the first 6 months.

Summaries

  • Recognized on a regular basis for outstanding performance and contributions to the Miscellaneous industry's success.
  • Dedicated to learning, growing, and succeeding in Miscellaneous.
  • Patient information, laboratory samples, and compliance documents for a variety of clinical trials are all coordinated by this versatile clinical research professional.
  • Within Miscellaneous, senior Research Study Coordinator and outstanding performer in risk assessment and stakeholder engagement.
  • Excellent track record of resolving issues, increasing customer satisfaction, and driving overall operational improvements.
  • Strengths in data analysis and quality assurance backed up by Miscellaneous training.
  • Achieved high retention rates.
  • Collaborative team leader with experience managing 3+ staff and multi-site trials, ensuring smooth communication between research sites at Denver.
  • Achieved no audit deficiencies.
  • Accomplished in securing research funding, contributing to obtaining $11 grants that expanded study scope and future trial opportunities.

Accomplishments

  • Implemented regulatory updates and protocol amendments across 3 studies, maintaining 100% compliance with IRB and GCP standards.
  • Troubleshot issues with digital data collection platforms, resulting in a 75% improvement in data accuracy and reducing lag times in reporting.
  • Effectively managed the coordination of multi-site trials, facilitating collaborations in 13 locations and improving the speed of data analysis.
  • Documented and resolved framework which led to standard.
  • Voluntarily took the lead in developing a centralized tracking system for patient visits, decreasing missed appointments by 30% and increasing adherence to the research schedule.
  • Led site initiation visits for 17 research sites, ensuring operational readiness and timely recruitment launches.
  • Collaborated with cross-functional teams to expedite study start-up timelines, cutting project launch delays by one year.
  • Delivered comprehensive progress reports to clinical and management teams, ensuring up-to-date status on 14 active studies and meeting all sponsor deliverables.
  • Led recruitment efforts that secured 5 participants in one year, achieving 18% of the study’s target sample size.
  • Developed a telemedicine platform usage guide, improving participant feedback response rates by 75% through better user instructions and support.

Affiliations

  • Project Management Institute
  • Association for Supply Chain Management (APICS)
  • Health Research Alliance (HRA)
  • American Medical Informatics Association
  • American Society of Clinical Oncology (ASCO)
  • Global Health Council (GHC)
  • Society of Human Resource Management
  • Collaborative Research Networks – Clinical Research Forum
  • Association for the Advancement of Medical Instrumentation (AAMI)
  • International Clinical Trials Society (ICTS)

Certifications

  • Certified Clinical Research Coordinator (CCRC) by ACRP
  • Human Subjects Protection (HSP) Certification by NIH
  • Society of Clinical Research Associates (SOCRA) Certified Clinical Research Professional (CCRP)
  • Fundamentals of Budgeting for Clinical Trials Certification by Vantage
  • Certified Public Accountant
  • Certified Clinical Research Project Manager by AAPM
  • FDA Clinical Investigator Training Certification
  • Bioethics Certification by method or Ironclad Systems
  • Remote Research Study Coordination Certification by method
  • Clinical Data Management Certification (CDM) by Northwind

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