Allison Colton
Prescott
Summary
Accomplished Clinical Research Associate with experience performing and documenting pre-study site evaluations, regulatory document collection, interim monitoring and study close-out visits. Diligent in performing studies aligned with good clinical practices, study-specific requirements and clinical monitoring plans. In-depth knowledge of company procedures, regulatory requirements and quality standards.
Overview
7
7
years of professional experience
Work History
Chemistry Teacher
Basis Education
07.2024 - Current
- Instructed students in lab by teaching safety protocols for proper use of chemicals and safe disposal of hazardous materials.
- Engaged students and promoted intellectual curiosity through hands-on experiments, PowerPoint presentations and mnemonics to provide positive attitude towards scientific processes.
- Evaluated and revised lesson plans and course content to achieve student-centered learning.
- Fostered motivating learning environment by planning and displaying enthusiasm for organic and inorganic chemistry.
- Leveraged varied instructional delivery modes to support student differences and learning styles.
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
Texas A&M University
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
Chemistry Teacher
Basis Education
07.2024 - Current
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
BS - Pre-Professional Biomedical Sciences
Texas A&M University
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