Clinical Research Associate

A client of Insight Global is looking for Clinical responsibilities include collecting clinical data and biological samples such as ECGs, vital signs, and venipuncture in accordance with study protocols and standard operating procedures. Accuracy checks are performed regularly, and source documentation is maintained diligently. Adverse events are monitored and promptly reported to medical staff. Research participants are guided and supported ethically and safely throughout their involvement. Visual examinations are conducted, and diagnostic devices are operated as needed. Biological samples are managed with care, including labeling, documentation, and inventory reconciliation. Participant intake is handled via phone, with a focus on maintaining database integrity. Ongoing clinical training is attended, and certifications are kept up to date to ensure compliance and quality care.

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Required Skills & Experience

2-3 years of experience in Clinical Research Trials

2-3 years of experience in Data Collection or Clinical Trials Assistant

Experience with GPD (Good Documentation practices)

Proficiency with MS Teams

Benefit packages for this role will start on the 31st day of employment and include medical, dental, and vision insurance, as well as HSA, FSA, and DCFSA account options, and 401k retirement account access with employer matching. Employees in this role are also entitled to paid sick leave and / or other paid time off as provided by applicable law.