- Cleveland, Ohio, United States
- On-site
- 1+ years
Responsibilities
- Participate in daily research project activities.
- Plan, organize, perform and monitor daily project protocols.
- Collect, prepare and maintain required research documentation, including informed consent records, case records, clinical notes and medical reports.
- Report and assist with managing protocol deviations, adverse events and other project-related issues.
- Be responsible for the general maintenance and upkeep of the lab.
Requirements
- High School Diploma or GED
- Associate's degree in laboratory science
- Bachelor’s degree
- Master’s degree
- Nice to have: independent execution of routine and semi-technical experiments