Clinical Research Technician

Katalyst CRO; Grayslake (IL); On-site; USD 35,000 - 50,000; Full time

Job summary

A leading clinical research organization is seeking a Clinical Research Coordinator to perform study protocol activities such as phlebotomy and ECG collection. This role requires a high school diploma and relevant medical experience, offering opportunities in a clinical environment.

Qualifications

• 1-2 years work experience in clinical/research environment.
• Experience with phlebotomy responsibilities is required.

Responsibilities

• Review protocols and comply with study-specific activities.
• Maintain accurate source data and perform phlebotomy tasks.
• Ensure safety and confidentiality of study subjects.

Skills

Phlebotomy

Lab work

ECG collection

Vital signs collection

Clinical and/or hospital experience

Education

High School Diploma or equivalent

Clinical Medical Assistant, EMT, Paramedic, military medic

Job description

Responsibilities

• Review protocols and comply with study-specific activities.
• Communicates in an appropriate and professional manner with study subjects and unit personnel.
• Maintain accurate and complete source data.
• Perform study protocol related activities, i.e. phlebotomy, sample processing, ECG collection, vital signs, height/weight, etc., as assigned.
• Maintain safety and confidentiality of study subjects throughout the study.
• Understands and comply with SOPs, FDA regulations, and basic GCP requirements.
  
  

Requirements:

• High School Diploma or equivalent.
• Clinical Medical Assistant, EMT, Paramedic, military medic with recent clinical experience, or higher.
• 1-2 years of work experience in a clinical or research environment, or in a patient care setting.
• 1-2 years of work experience in a role with phlebotomy responsibilities.
  
  

Top Skills:

• Phlebotomy.
• Lab work.
• ECG collection.
• Vital signs collection.
• clinical and/or hospital experience.