Clinical Research Coordinator II

Job overview

The Clinical Research Coordinator II role is onsite in Gilbert, AZ. Compensation is not specified. The coordinator supports clinical trial activities and works with study teams, clinics, sponsors, and research participants to meet protocol objectives and company goals.

What you'll do

• Coordinate multiple concurrent trials
• communicate with study team members and serve as a clinic and sponsor contact for clinic activities
• schedule participants and collect histories
• maintain source documentation, study documents, and reports
• enter data and resolve queries
• conduct informed consent
• coordinate study procedures, visits, and follow-up
• support screening, recruitment, and enrollment
• collect, process, and ship specimens
• report adverse events
• and support study initiation, monitoring, and close-out.

What we're looking for

Skills & competencies

clinical research coordinator ii

clinical trials

research participants

informed consent

study documentation

data entry

specimen processing

gcp

gilbert az

elligo health research

travel varies by position

Work arrangement

• Weekend coverage required

Why this role

Requires at least three years of clinical trial coordination experience and a bachelor’s degree in life science or a related discipline, or equivalent work experience. Travel is stated as 50% for traveling positions and 15–25% for non-traveling positions; the listing does not specify which applies.

About the employer

ELLIGO HEALTH RESEARCH INC is hiring for this role. Industry: Research and Development in the Physical, Engineering, and Life Sciences (except Nanotechnology and Biotechnology). Sector: 54.