Kayelee Auer
Summary
Versatile clinical research professional knowledgeable about coordinating patient information, laboratory samples and compliance documents for diverse clinical trials. Highly organized and thorough with good planning and problem-solving abilities. Certified in phlebotomy, GCP and IATA.
Overview
5
5
years of professional experience
1
1
Certification
Work History
Clinical Research Coordinator
Cedar Clinical Research
06.2023 - Current
- Enhanced patient safety by meticulously monitoring and documenting adverse events during clinical trials.
- Streamlined data collection processes for increased efficiency and accuracy in study results.
- Coordinated with cross-functional teams to ensure timely completion of clinical trial milestones.
- Improved recruitment rates by developing and implementing effective patient outreach strategies.
- Facilitated clear communication between principal investigators, sponsors, and study participants for seamless trial execution.
- Maintained compliance with regulatory guidelines through rigorous documentation and protocol adherence.
Clinical Research Assistant
Intermountain Health
11.2021 - 05.2023
- Streamlined data collection processes for improved accuracy and efficiency in clinical research projects.
- Managed study databases, ensuring accurate data entry, storage, and retrieval for analysis purposes.
- Provided training to new team members on proper procedures for data collection, documentation, and reporting in clinical trials.
- Participated in site monitoring visits, addressing any concerns or discrepancies related to patient enrollment or data collection procedures.
- Screened patient records, databases, and physician referrals to identify prospective candidates for research studies.
- Followed informed consent processes and maintained records.
Clinical Research Coordinator
Psychiatric & Behavioral Solutions
07.2019 - 11.2021
- Coordinated with cross-functional teams to ensure timely completion of clinical trial milestones.
- Enhanced patient safety by meticulously monitoring and documenting adverse events during clinical trials.
- Streamlined data collection processes for increased efficiency and accuracy in study results.
- Managed study budgets and resources to maximize return on investment while maintaining quality standards.
- Developed strong relationships with trial sponsors, ensuring ongoing collaboration and future project opportunities.
- Oversaw the management of investigational product supplies, ensuring appropriate storage conditions were maintained at all times for optimal efficacy during trials.
- Assessed patients'' eligibility criteria following strict adherence to inclusion/exclusion guidelines.
- Collected data and followed research protocols, operations manuals, and case report form requirements.
- Participated in initiation visits and investigator meetings, implementing trials in accordance with study timelines and budgets.
- Gathered, processed, and shipped lab specimens.
- Maintained compliance with protocols covering patient care and clinical trial operations.
Education
Associates of Science -
Salt Lake Community College
03.2024
Skills
- Specimen handling
- Specimen collections
- Research experience
- Informed consent
- Trial management
- Participant screening
- Medication Dispensing
- Phlebotomy
- Good Clinical Practices
- Research SOPs understanding
- Study protocols
- Data collection techniques
- Schedule Coordination
Personal Information
Title: Clinical Research Coordinator
Certification
- Phlebotomy Training -2021
- GCP Training -June 2023
- IATA Training - June 2023
Timeline
Clinical Research Coordinator
Cedar Clinical Research
06.2023 - Current
Clinical Research Assistant
Intermountain Health
11.2021 - 05.2023
Clinical Research Coordinator
Psychiatric & Behavioral Solutions
07.2019 - 11.2021
Associates of Science -
Salt Lake Community College
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