Job Description

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

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