Clinical Research Associate (CRA) I at Katalyst Healthcares Life Sciences
Grayslake, IL 60030, USA -
Full Time


Start Date

Immediate

Expiry Date

28 Nov, 25

Salary

0.0

Posted On

28 Aug, 25

Experience

1 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Phlebotomy, Emt

Industry

Hospital/Health Care

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 complies 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.

Note:

  • Open 24/7, will work 8-hour shifts. There is no guarantee of hours. Some weeks may have no shifts whereas others may have 4 or 5. Shift options: day shift for training, then AM/PM and weekend availability for contract. Schedule comes out every 2 weeks.
  • Name of Functional Area/Department: Clinical Pharmacology & Pharmacometrics Research Unit.

Top Skills:

  • Phlebotomy.
  • Lab work.
  • ECG collection.
  • Vital signs collection.
  • clinical and/or hospital experience.
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 complies with SOPs, FDA regulations, and basic GCP requirements
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