Role Summary
The opportunity is to serve as an integral member of the site and study team during study processes, including pre-admit, admission, orientation, conduct, discharge and study close. The role supports research activities in a clinical environment, requiring adherence to protocols and regulatory standards.
Responsibilities
- Performs conduct procedures in strict compliance to the study protocol, Good Clinical Practice standards, Standard Operating Procedures (SOPs), QA/QC procedures, OSHA guidelines and other state and local regulations as applicable
- Provides assistance in the execution of clinical trials
- Ensures the well-being and safety of study participants
- Provides administrative and operational support
Qualifications
- Required: High school diploma or GED and phlebotomist certification
- Required: 1–2 years of experience in a clinical environment
Skills
- Able to obtain vital signs and perform ECGs
- Able to perform telemetry and insertion of intravenous catheters, or a willingness to learn
- Excellent oral, written and interpersonal communication skills
- Able to work independently and handle multiple competing priorities
- Able to work with tight deadlines
- Able to function independently within a team environment
- Excellent organizational and time-management skills and a strong attention to detail
- Proficient in MS Office Suite (Word, Excel, Outlook)
Education
- High school diploma or GED and phlebotomist certification