Role OverviewResponsible for the collection, coordination, processing and quality control of clinical trial data. May assist with screening patients for research protocols.
What You Will Do
Assist the Research Coordinator in the coordination of studies, assist in daily clinical trial activities, schedule study participant appointments, and extract data from patient charts.
Why It Might Be a Fit
Requires strong critical thinking and problem-solving skills, ability to work under pressure, and excellent interpersonal skills.
Requirements
- High attention to detail and strong organizational skills
- Excellent written and verbal communication skills
- Ability to work well independently
- Maintain confidentiality
- Experience with Microsoft Office Suite (Outlook, Word, Excel, PowerPoint)
- Possess strong skills for multitasking, meeting competing deadlines, prioritizing and supporting PIs for multiple projects
- Experience performing ECGs
- Experience with venipuncture
- Prior office experience
- Prior Clinical Research-related experience in human trials
Benefits
- Dental insurance
- Vision insurance
- Health insurance
- Paid time off
- Retirement plan
- Life insurance
- Disability insurance
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