Clinical Research Coordinator - Drive Inclusive Health Research

Howard Brown; Chicago (IL); On-site; USD 62,000 - 68,000; Full time

Benefits offered by this job

Health insurance

Dental insurance

Vision insurance

401k with employer match

Life insurance

Disability insurance

Commuter benefits

Flexible Spending Accounts

Tuition reimbursement

Employee assistance program

PTO and sick days

Job summary

Howard Brown Health in Chicago, IL is seeking a Clinical Research Coordinator to support ongoing trials, prepare study documents, and ensure GCP/ICH/FDA compliance. You will coordinate regulatory tasks, assist investigators, and communicate with sponsors.

The role involves data collection, patient visits, and documentation management, contributing to high-quality research in LGBTQ+ health. A strong writing/organization skill set and experience in clinical research are required.

Qualifications

• B.S. or B.A. with 2+ years clinical research experience
• A.A. or A.S. with 5+ years clinical research experience
• High School Diploma/Equivalent with 8+ years clinical research experience
• Strong writing and communication skills
• Ability to organize and manage multiple tasks efficiently
• Working knowledge of general medical terminology and regulatory guidelines

Responsibilities

• Provide study coordination for assigned trials under the Clinical Research Manager
• Assist with regulatory paperwork for IRB submissions and annual reviews
• Ensure timely reporting of SAEs to IRB and sponsor
• Create and update regulatory binders for studies
• Schedule patient visits and coordinate data collection and entry
• Interact with sponsors and investigators as a study representative
• Maintain study records and assist with recruitment and retention activities

Skills

Clinical research experience

Strong writing

Organization skills

Communication skills

Attention to detail

Prioritization

Regulatory knowledge

Medical terminology

Multitasking

IRB coordination

Education

Bachelor's or higher + 2+ years clinical research

Associate degree + 5+ years clinical research

High school diploma + 8+ years clinical research

Job description

Howard Brown Health in Chicago, IL is seeking a Clinical Research Coordinator to support ongoing trials, prepare study documents, and ensure GCP/ICH/FDA compliance. You will coordinate regulatory tasks, assist investigators, and communicate with sponsors.

The role involves data collection, patient visits, and documentation management, contributing to high-quality research in LGBTQ+ health. A strong writing/organization skill set and experience in clinical research are required.