Clinical Research Coordinator II — Trials, Compliance & Impact

Loyola University Chicago; Chicago (IL); On-site; USD 37,195 - 42,705; Full time

Job summary

A prominent educational institution in Chicago is seeking a Clinical Research Coordinator II to manage multiple research protocols efficiently. This role includes data collection, participant interaction, and compliance with regulations. The ideal candidate should possess a Bachelor's degree and 2-5 years of relevant experience, along with strong organizational skills and knowledge of clinical practices. Salary ranges from $27/hr to $31/hr, with a focus on maintaining high standards in clinical research operations.

Qualifications

• 2-5 years of previous job-related experience required.
• Must interact with study participants and manage data according to protocols.

Responsibilities

• Coordinate clinical trials ensuring compliance with protocols.
• Manage data collection, patient interaction, and study documentation.
• Prepare regulatory submissions and manage relationship with IRB.

Skills

Ability to follow oral and written instructions

Knowledge of regulatory compliance

Medication administration

Basic knowledge in Excel and WORD

Education

Bachelors Degree or equivalent training

Tools

Excel

EPIC (EMR)

Job description

A prominent educational institution in Chicago is seeking a Clinical Research Coordinator II to manage multiple research protocols efficiently. This role includes data collection, participant interaction, and compliance with regulations. The ideal candidate should possess a Bachelor's degree and 2-5 years of relevant experience, along with strong organizational skills and knowledge of clinical practices. Salary ranges from $27/hr to $31/hr, with a focus on maintaining high standards in clinical research operations.