Responsibilities
Under the direction of the PI (Principal Investigator) site management team, clinical research coordinator, research assistants may be responsible for any/all of the following:
- Clinical trial protocol knowledge and study
- Participant recruitment
- Customer service
- Data entry
- Chart Screening
- Coordinating study visits
- Potentially assisting with samples
- Maintaining subject binders
- Supply management
- Processing volunteers
- Taking biological samples or vital signs
- Organizing data
Requirements
- High school diploma or equivalent
- Strong Customer Service Skills
- Excellent communication skills; both written and verbal
- Ability to work independently as well as in a team environment
- Reliable transportation
- Flexible Hours
Preferred Qualifications
- Medical terminology
- Medical clinic experience
- Sound computer and technology experience
- Strong verbal and electronic communication skills