Elizabeth Schaeper
West Chester,OH
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 Clinical Research Coordinator.
Overview
7
7
years of professional experience
1
1
Certification
Work History
Clinical Research Coordinator
Velocity Clinical Research
08.2021 - Current
- Contributed to the successful completion of clinical trials by proactively resolving issues, mitigating risks, and meeting deadlines in a fast-paced environment.
- Enhanced patient safety by meticulously monitoring and documenting adverse events during clinical trials.
- Developed strong relationships with trial sponsors, ensuring ongoing collaboration and future project opportunities.
- Trained new team members on essential clinical research protocols and procedures, promoting a culture of continuous learning.
- Assessed patients'' eligibility criteria following strict adherence to inclusion/exclusion guidelines.
- Screened patient records, databases, and physician referrals to identify prospective candidates for research studies.
- Followed clinical research protocols and conducted study visits in compliance with ICH/GCP and FDA regulations.
- Facilitated clear communication between principal investigators, sponsors, and study participants for seamless trial execution.
- Gathered, processed, and shipped lab specimens.
- Increased participant retention rates through proactive follow-up efforts and regular engagement activities.
- Skilled at working independently and collaboratively in a team environment.
- Learned and adapted quickly to new technology and software applications.
- Prepared detailed informed consent documents to clearly communicate risks, benefits, expectations, rights and responsibilities related to participation in clinical trials.
Outreach Phlebotomist
University Of Cincinnati
12.2016 - 08.2021
- Protected patients by following infection control, sharps disposal, and biohazardous waste disposal procedures.
- Performed venipunctures for both adult and pediatric patients.
- Promoted a safe and clean work environment by adhering to strict infection control protocols.
- Adapted quickly to changing workflows and patient needs during high-volume periods, maintaining a calm and professional demeanor.
- Streamlined the specimen collection process, reducing wait times for patients and improving overall efficiency.
- Ensured proper specimen labeling and handling procedures were followed to maintain sample integrity throughout the testing process.
- Assisted in training and onboarding new phlebotomists.
- Collected blood samples using vacutainer tubes, tourniquets, syringes, butterfly needles, and straight needles.
Education
High School Diploma -
Lakota West High School
West Chester, OH05.2012
Skills
- Documentation Management
- Report Preparation
- Phlebotomy
- Study protocols
- Participant screening
- Specimen handling
- Research experience
- Medication Dispensing
- Informed Consent Process
- Patient recruitment
- Adverse event reporting
- Microsoft Office
- Organizational Skills
- First Aid/CPR
Certification
- Certified Clinical Research Coordinator - OCT 2023
Timeline
Clinical Research Coordinator
Velocity Clinical Research
08.2021 - Current
Outreach Phlebotomist
University Of Cincinnati
12.2016 - 08.2021
High School Diploma -
Lakota West High School
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