Clinical Research Coordinator - ProHealth Care
(2024-09 - 2025-09)
Temporary (One year project). Hybrid role; worked independently and as a team member.
- Recruited, screened, collected and entered data, and performed all other aspects of study requirements.
- Organized and maintained complete records of each study.
- Remained current with all required training.
- Prepared protocol worksheets and other study related documents.
Clinical Research Coordinator - Ascension
(2023-04 - 2024-09)
- Recruited, screened, collected and entered data, and responded to applicable queries to reconcile data.
- Maintained testing environments suitable for study requirements.
- Monitored active studies to maintain compliance.
- Documented adverse events and reports as necessary.
Covid-19 Screener - UW-Health, Madison
(2020-10 - 2021-10)
Temporary (One year contract).
- Utilized tympanic and oral thermometers to take and interpret patient temperatures, according to manufacturer's instructions.
- Administered medical questionaires to all visitors and personnel entering and departing job sites.
- Adhered to established protocols and reporting requirements in recording positive and negative cases.
- Enforced rules pertaining to mask wearing in designated areas of job site.
- Recorded details of screening results in an organizational database with accuracy and appropriate follow-up.
- Managed proper sanitization of screening stations and other work areas, adhering closely to established procedures and standards.
- Disinfected surfaces and equipment regularly to protect patients and staff from infection.
Clinical Research Coordinator - SSM Health, Madison, Wi
(2014-01 - 2019-08)
- Communicated with study participants, family members, and other contacts to offer information and resources.
- Established set up and maintained testing environments suitable for study type.
- Prepared study reports and annual review documents.
- Supported staff by assisting with program meeting coordination.
- Managed documentation, including clinical research data worksheets, shared drive, and clinical research files.
- Developed and implemented recruitment strategies to attract ample participation.
- Oversaw subject enrollment, verifying obtainment and documentation of informed consent.
- Screened potential subjects, reviewed medical records, and discussed histories with physicians or nurses to determine which individuals should be admitted to each study.
- Prepared the protocol worksheets, and other study related documentation.
- Performed study related tasks including EKG tracing, vitals, and phlebotomy.
Study Technician - Covance, Madison, Wi
(2000-06 - 2013-11)
- Maintained strict standards in verifying clinical information and communicating specimen procurement methods or techniques with patients.
- Verified recorded and reported results on all tests performed in compliance with government requirements and internal lab procedures.
- Verified sample and specimen labeling and processing against standards with regular quality checks.
- Followed all lab instrument procedures and guidelines, kept lab clean, and routinely calibrated instruments for precision.
