Senior Research Study Coordinator - Multi-Site Trials

Northwestern University; Chicago (IL); On-site; USD 66,477,465 - 83,067,902; Full time

Job summary

Northwestern University in Chicago, IL, seeks a Research Study Coordinator in the MED-Physical Med & Rehab department to manage day-to-day administrative and technical activities for complex national studies across multiple sites. You will ensure adherence to Good Clinical Practices, IRB, FDA CFR, and ICH guidelines throughout the study lifecycle.

Responsibilities include study planning, recruitment, informed consent, data collection and analysis, budget oversight, and preparation of reports for

Qualifications

• Bachelor's or master's degree in a related field or equivalent combination of education and experience.
• Must complete NU's IRB CITI training before interacting with participants and recertify every 3 years.

Responsibilities

• Participates in planning and conduct of research studies.
• Reviews project and protocol and recommends strategies to expedite the study.
• Recruits and retains participants; obtains informed consent.
• Administers tests and questionnaires following protocols.
• Collects, compiles, tabulates and processes responses.
• Gathers information and analyzes data from medical charts.
• Performs basic clinical procedures as needed.
• Manages study databases and ensures data is collected and entered correctly.
• Creates reports and summaries for publications and grant applications.

Skills

Informed consent administration

Participant recruitment

Data collection & analysis

Regulatory compliance (GCP/IRB)

Education

Bachelor's degree in social or health science

Master's degree in social or health science

Job description

Northwestern University in Chicago, IL, seeks a Research Study Coordinator in the MED-Physical Med & Rehab department to manage day-to-day administrative and technical activities for complex national studies across multiple sites. You will ensure adherence to Good Clinical Practices, IRB, FDA CFR, and ICH guidelines throughout the study lifecycle.

Responsibilities include study planning, recruitment, informed consent, data collection and analysis, budget oversight, and preparation of reports for