Research Assistant - Data, Lab Ops & Phlebotomy

Metro Infusion Center

Burr Ridge, Northern (IL, KY)

Hybrid

USD 23,000 - 32,000

Full time

14 days+
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Benefits offered by this job

401(k)
Dental insurance
Disability insurance
Health insurance
Life insurance
Paid time off
Retirement plan
Vision insurance

Job summary

Metro Infusion Center is seeking a Research Assistant under the supervision of the Director of Research to support non-clinical data collection across multiple projects. Responsibilities include data entry, analysis of clinical data, and ensuring adherence to study protocols and objectives.

The role involves setting up and calibrating research equipment, assisting monitors, handling lab samples, uploading documents to EMR, and coordinating with sponsors and CRAs.

Qualifications

  • High school diploma required; degrees in social sciences or health-related fields preferred.
  • Phlebotomy experience preferred.
  • Experience in the medical field preferred but not required.
  • Proficiency with Microsoft Office and EMR systems preferred.

Responsibilities

  • Enter data proficiently into a data capture system for sponsors and CROs.
  • Set up, calibrate, and maintain lab/field research equipment as required.
  • Assist Clinical Research Associates monitoring studies (on- and off-site).
  • Invoice payments for the clinical trial budget.
  • Ship lab samples following regulations and protocols.
  • Upload study documents to EMR chart and track specimen shipments.
  • Attend project meetings and communicate with staff via email/phone.
  • Perform ECGs and phlebotomy as needed.

Skills

Data entry
Phlebotomy
Medical field experience
Microsoft Office
EMR proficiency

Education

High school diploma
Degree in health-related discipline

Tools

Microsoft Office Suite
EMR systems

Job description

Metro Infusion Center is seeking a Research Assistant under the supervision of the Director of Research to support non-clinical data collection across multiple projects. Responsibilities include data entry, analysis of clinical data, and ensuring adherence to study protocols and objectives.

The role involves setting up and calibrating research equipment, assisting monitors, handling lab samples, uploading documents to EMR, and coordinating with sponsors and CRAs.

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