Pediatrics & Family Medicine Clinical Research Associate

1100 Endeavor Health Clinical Operations; Evanston (IL); Presencial; USD 59.000 - 89.000; Tempo integral

Benefícios oferecidos por esta vaga

Annual incentive plan

Shift and holiday pay

Tuition reimbursement

Free parking

Health Savings Account options

Resumo da vaga

1100 Endeavor Health Clinical Operations is seeking a Clinical Research Associate to oversee pediatric and family medicine studies in Evanston, IL. The CRA will manage human-subject research across multiple sites, ensuring IRB compliance and data integrity while coordinating with investigators and staff.

Responsibilities include recruiting, consenting, maintaining regulatory documents, and supporting grant submissions. Travel may be required as part of site coordination and trial oversight.

Qualificações

• Bachelor's degree in a relevant health-related field is required.
• Strong organizational, time management and communication skills needed.
• Experience in clinical research coordination is preferred.

Responsabilidades

• Ensure compliance with federal, state, local IRB and GCP regulations.
• Support clinical research across Pediatrics and Family Medicine.
• Coordinate recruitment, consent, and data collection at multiple sites.
• Prepare IRB submissions, amendments, and progress reports.
• Oversee data quality, entry, and documentation accuracy.
• Collaborate with investigators, sponsors, and study staff.
• Assist with grant submissions and protocol development.
• Monitor study progress, timelines, and budget considerations.

Conhecimentos

Organization

Time management

Problem solving

Communication

Independent work

EPIC

Workday

Formação

Bachelor's degree in biology/health science

Ferramentas

EPIC

Workday

Descrição da vaga

1100 Endeavor Health Clinical Operations is seeking a Clinical Research Associate to oversee pediatric and family medicine studies in Evanston, IL. The CRA will manage human-subject research across multiple sites, ensuring IRB compliance and data integrity while coordinating with investigators and staff.

Responsibilities include recruiting, consenting, maintaining regulatory documents, and supporting grant submissions. Travel may be required as part of site coordination and trial oversight.