Remote-Eligible Research Project Manager

Hugh Chatham Health; Oak Brook (IL); Hybrid; USD 79,000 - 119,000; Full time

Benefits offered by this job

Health benefits

Paid time off

Retirement plans

Educational assistance

Job summary

Advocate Health is seeking an experienced Research Project Manager in Oak Brook, IL. The role focuses on planning, executing, and overseeing pragmatic clinical trials and multi-site research studies with cross-functional teams.

You will coordinate timelines, recruitment, and reporting while ensuring adherence to GCP, ICH, FDA CFR, IRB, and institutional guidelines; collaborate with leaders across departments and external partners.

Qualifications

• Knowledge of health services research and recruitment processes.
• Ability to lead multi-site, multi-stakeholder projects with accuracy.
• Strong communication and leadership capabilities.

Responsibilities

• Lead planning, execution, and oversight of pragmatic clinical trials and research studies.
• Manage timelines and ensure recruitment and reports are on schedule.
• Track progress and provide status updates to collaborators.
• Develop project plans, charters, reports, and implementation strategies.
• Coordinate activities among clinical, IT, and research teams and external partners.
• Build relationships with research teams and assist in new proposals.
• Ensure study activities follow GCP, ICH, FDA CFR, IRB and related guidelines.

Skills

Project management

Leadership

Communication skills

Research coordination

IRB knowledge

REDCap

Microsoft Excel

Mentoring staff

Team collaboration

Problem solving

Education

Master's Degree in Business or related field

Master's Degree in Health Science or related field

Tools

REDCap

Microsoft365 (Excel)

Job description

Advocate Health is seeking an experienced Research Project Manager in Oak Brook, IL. The role focuses on planning, executing, and overseeing pragmatic clinical trials and multi-site research studies with cross-functional teams.

You will coordinate timelines, recruitment, and reporting while ensuring adherence to GCP, ICH, FDA CFR, IRB, and institutional guidelines; collaborate with leaders across departments and external partners.