Allison Colton
Prescott,AZ
Summary
Analytical Clinical Research Associate well-versed in coordinating operations, managing sites and drafting detailed clinical reports. Knowledgeable about action planning, database locking and standard operating procedures. Supports participant recruitment and management to meet research objectives.
Overview
5
5
years of professional experience
Work History
Clinical Research Associate, Rare Disease
IQVIA
08.2021 - 10.2023
- Maintained site monitoring schedules to facilitate effective communication with members of clinical team.
- Reviewed clinical data, source documentation, case report forms, and investigative site regulatory files to verify accuracy and completion.
- Conducted 9 days of initiation,180 days of monitoring, and 50 days of closeout visits to verify study procedures, regulatory documents, and data completion.
Clinical Research Coordinator, Post-Operative Pain
Arizona Research Center
03.2021 - 08.2021
- 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.
Clinical Research Coordinator, Hematology Oncology
Mayo Clinic
06.2019 - 03.2021
- Coordinated and monitored clinical trial activities for 15 trials to support timely and accurate completion of studies.
- Worked with principal investigators and sponsors to facilitate daily trial activities and comply with research protocols.
Clinical Research Coordinator, Neurology
Xenoscience Inc.
06.2018 - 06.2019
- Managed patient recruitment, informed consent process and data entry to support trial objectives.
- Oversaw management of investigational product supplies, ensuring appropriate storage conditions were maintained at all times for optimal efficacy during trials.
Education
BS - Pre-Professional Biomedical Sciences
05.2017
Skills
- Site Management
- Pharmacovigilance
- Biostatistics knowledge
- Detailed documentation
- Electronic Data Capture
- ICH Guidelines
- Informed Consent Process
- Adverse event reporting
- Completing regulatory documents
- Source Document Verification
References
References available upon request
Timeline
Clinical Research Associate, Rare Disease - IQVIA
08.2021 - 10.2023
Clinical Research Coordinator, Post-Operative Pain - Arizona Research Center
03.2021 - 08.2021
Clinical Research Coordinator, Hematology Oncology - Mayo Clinic
06.2019 - 03.2021
Clinical Research Coordinator, Neurology - Xenoscience Inc.
06.2018 - 06.2019
Texas A&M University - BS, Pre-Professional Biomedical Sciences