Amy Beitzel
Akron
Summary
Skilled clinical research coordinator with background in managing and overseeing clinical trials. Experience includes coordinating with research teams, ensuring compliance with protocols, and managing participant recruitment and data collection processes. Possess strong organizational skills, ability to manage multiple tasks efficiently, and capability to ensure accuracy in documentation and reporting. Excel at communication, teamwork, and problem-solving, using these soft skills to navigate challenges and drive projects to completion. Contributed to improving trial procedures and enhancing data integrity in previous roles.
Overview
8
8
years of professional experience
1
1
Certification
Work History
Clinical Research Coordinator
Summa Health-Akron City Hospital
Akron
05.2022 - Current
- Evaluated complex research protocols and developed concise testing and scheduling guidelines for multi-year studies.
- Worked with principal investigator and sponsors to facilitate daily trial activities and comply with research protocols.
- Identified potential research candidates through patient database reviews in the EPIC EHR.
- Utilized EPIC reporting functions to maintain recruiting and enrollment records.
- Updated research schedules and documentation, as indicated by protocol amendments.
- Entered study data into study-specific portals, including imaging and cardiac management systems.
- Researched and responded to study eCRF inquiries in a timely manner to facilitate data accuracy and compliance.
- Maintained accurate visit billing per schedules of events, add-on visits, and cost analysis reviews in Advarra Clinical Conductor.
- Prepared and maintained regulatory documents for clinical trial submissions, including IRB submissions, and clinical safety data reports.
- Prepared document reviews for research study monitors, including the release of records access in EPIC.
- Participated in initiation visits and investigator meetings, implementing trials following study timelines and budgets.
- Developed strong relationships with trial sponsors, ensuring ongoing collaboration, and future project opportunities.
- Trial Lead: PNK02 Proaction
- Trial Lead: Nucleix LUNG- RND - 003
Clinical Research Coordinator - NeuroCare Center
Ohio Clinical Research Partners, LLC,
North Canton
06.2017 - 06.2018
- Alkermes 8700-A302; Alkermes 8700-A301
- Eisai E2609- G000- 301; Eisai E2609- G000- 202
- Suven Life Sciences Ltd
- Merck 8931-019 (Prodromal AD)
Education
Bachelor of Arts - Applied Communication
Kent State University
Kent, OH08-2012
LPN License - Nursing
W. Howard Nicol School of Practical Nursing
Akron, OH09-2007
Skills
- EPIC "Superuser" 2017; inpatient and ambulatory
- Clinical trial management
- Clinical Protocol Compliance
- Regulatory compliance
- Protocol review
- Safety reporting
- Investigator coordination
- Collaboration with sponsors
- Visit billing
- Documentation management
- Data entry
- Problem-solving abilities
- Time management abilities
- Excellent communication
- Adaptability and flexibility
- Analytical thinking
Certification
- Ohio Nursing Licensure LPN.127968.MEDS-IV
Nursing Experience
- LPN Clinical Team and Patient Navigator – Summa Weight Management Institute 2020-2022
- LPN Staff Nurse – Summa Rehab Hospital 2018-2020
- LPN Staff Nurse – Acute Palliative Care Unit 2007-2017
Timeline
Clinical Research Coordinator
Summa Health-Akron City Hospital
05.2022 - Current
Clinical Research Coordinator - NeuroCare Center
Ohio Clinical Research Partners, LLC,
06.2017 - 06.2018
Bachelor of Arts - Applied Communication
Kent State University
LPN License - Nursing
W. Howard Nicol School of Practical Nursing
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