Full-Time

Clinical Research Nurse

Posted on 12/25/2025

Deadline 3/16/26
University of Chicago

University of Chicago

Compensation Overview

$70k - $100k/yr

Chicago, IL, USA

In Person

Category
Medical, Clinical & Veterinary (1)
Required Skills
Data Analysis
Requirements
  • A college or university degree in related field.
  • Knowledge and skills developed through 2-5 years of work experience in a related job discipline.
Responsibilities
  • Recruits and retains research subjects for clinical studies; Provides all necessary support during studies. Administer informed consent.
  • Assists PI and other investigators in preparation and submission of IRB regulatory materials, preparation and submission of OSR documents (including consent forms), maintenance of records according to all regulations.
  • Coordinates collecting, compiling, tabulating &/or processing responses; gathering information; &/or assisting in the preparation of material for inclusion in reports and journals. Assists with submission to journals.
  • Assists with processing subject reimbursement materials.
  • Assists PI with other mandatory regulatory and compliance areas such as CT.Gov.
  • Applies logic and reasoning to identify the strengths and weaknesses of alternative solutions, conclusions or approaches to problems.
  • Interprets information from caregivers, nurses, or physicians about patient condition, treatment plans, or appropriate activities.
  • Performs other related work as needed.
Desired Qualifications
  • Bachelor's degree.
  • Previous experience in observational and interventional clinical research.
  • Prior clinical experience with persons with diabetes.
  • CITI, GCP, HIPAA training.
  • Advanced medical terminology.
  • Knowledge of research techniques or methods.
  • Knowledge of regulatory policies and procedures.
  • Knowledge of patient care fundamentals, including aseptic principles and techniques.
  • Ability to interact professionally with a wide range of internal and external contacts from faculty investigators study teams, regulatory staff, IRB personnel, site visitors, sponsor monitors, et al.
  • Ability to review complex clinical research protocols and identify regulatory, ethical or feasibility issues.
  • Ability to provide direct care in a professional and respectful manner.
  • Analytical and problem-solving skills, attention to detail and organizational skills.
  • Excellent verbal and written communication.
  • Ability to read documents or instruments.
  • Ability to perform multiple concurrent tasks with occasional interruptions.
  • Ability to exercise discretion and confidentiality while handling sensitive situations.
  • Ability to solve problems by applying math or reasoning principles.
  • Ability to adapt to changing working situations and work assignments.
  • Ability to work independently and as part of a team.
  • A working knowledge of Microsoft Office software.
  • Strong phlebotomy and venous access (IV) skills.
University of Chicago

University of Chicago

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