Hayden Krause
Jackson
Summary
Personable and reliable, with strong foundation in clinical research practices and patient care. Well-versed in regulatory compliance and data management, with solid grasp of clinical trial protocols. Dedicated to ensuring patient safety and efficiency of clinical research projects and contributing to meaningful advancements in oncology research.
Overview
9
9
years of professional experience
Work History
Clinical Research Coordinator III/Disease Team Lead
Medical College of Wisconsin
09.2022 - Current
- Job duties listed below for clinical research assistant, clinical research coordinator I, amd clinical research coordinator II:
- Increase in overall patient/study workload
- Team-wide management of protocol amendments and continuing progress reviews with site IRB
- Serve as acting manager when team manager is unavailable
- Determine workload assignment and time management for the disease team manager
Study Chair Liaison
Medical College of Wisconsin
12.2021 - Current
- Facilitate Communication: Act as a central point of contact between study sites, National Cancer Institute (NCI), corroborating laboratories, and study chair
- Protocol Development: In collaboration with NCI and study chair, develop clinical trial protocol and consent documents for NCI central IRB approval
- Project Support: Provide support to participating sites by tracking progress and disseminating status updates to NCI, study chair, and study sites
- Protocol Information Management: Keep all relevant parties informed about protocol updates and study chair decisions
- Ensure all necessary documentation is organized and readily available as needed
Clinical Research Coordinator II
Medical College of Wisconsin
03.2020 - 08.2022
- Job duties listed below for both clinical research assistant and clinical research coordinator I:
- Aid in training and development of new hires and newly promoted clinical research coordinators
- Develop and implement improved training materials, create improved processes to increase team efficiency and patient recruitment
- Increase in overall patient/study workload
Clinical Research Coordinator I
Medical College of Wisconsin
07.2016 - 03.2020
- Job duties listed below for clinical research assistant:
- Followed clinical research protocols and conducted study visits in compliance with ICH/GCP and FDA regulations.
- Oversee subject enrollment to ensure that informed consent is properly obtained and documented
- Interpret protocols and advise treating physicians on appropriate dosage modifications or treatment calculations based on patient characteristics
- Maintain frequent contact with study sponsors to coordinate and conduct site initiation visits, on-site and remote monitoring visits, and close out visits, provide HIPPA compliant source documentation, and facilitate IRB approval of study protocols/amendments
- Utilize a vast array of vendor systems including but not limited to Florence, Oncore, Vestigo, Microsoft 365 Suite, Medidata RAVE, Clario Global/SMART, LabCorp, Signant IRT
Clinical Research Assistant
Medical College of Wisconsin
11.2015 - 07.2020
- Maintain required records of study activity including case report forms, drug dispensation records, or regulatory forms
- Record adverse events and concomitant medications data and confer with investigators regarding the reporting of events to oversight agencies
- Prepare study-related documentation such as protocol worksheets, procedural manuals, adverse event reports, institutional review board documents, and progress reports
- Code, evaluate, or interpret collected study data
- Direct the requisition, collection, labeling, storage, or shipment of specimens
- Maintain and enforce HIPPA compliance with all study related patients and data
Education
Biomedical Sciences/Pre-Medicine - Double-minor in Chemistry and Nutrition
University of Wisconsin - La Crosse
La Crosse, WI05.2015
High School Diploma -
Hartford Union High School
Hartford, WI06.2010
Skills
- Good clinical practices
- Ability to efficiently multitask
- Strategic leadership
- Clinical trial management
- Fast and Independent Learner
Credentials And Licenses
- CITI/GCP Certification, 11/15 - Present
- SoCRA Certification, 04/19 - 03/22
Accomplishments
Authorship – “A Pilot Clinical Study to Investigate the Hypomethylating Properties of Freeze-dried Black Raspberries in Patients with Myelodysplastic Syndrome or Myeloproliferative Neoplasm”
Timeline
Clinical Research Coordinator III/Disease Team Lead
Medical College of Wisconsin
09.2022 - Current
Study Chair Liaison
Medical College of Wisconsin
12.2021 - Current
Clinical Research Coordinator II
Medical College of Wisconsin
03.2020 - 08.2022
Clinical Research Coordinator I
Medical College of Wisconsin
07.2016 - 03.2020
Clinical Research Assistant
Medical College of Wisconsin
11.2015 - 07.2020
High School Diploma -
Hartford Union High School
Biomedical Sciences/Pre-Medicine - Double-minor in Chemistry and Nutrition
University of Wisconsin - La Crosse
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