Kendra Elmer

Temporary (One year project). Hybrid role; worked independently and as a team member.

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.

Bachelor of Arts - Sociology - Oklahoma Baptist University (1999-12)