Impactful Clinical Research Coordinator

St. Elizabeth HealthCare; Elizabeth, Northern (NJ, KY); Hybrid; USD 65,000 - 90,000; Full time

Benefits offered by this job

Competitive pay

Health coverage within 30 days

Paid time off

Retirement plan with employer match

Tuition reimbursement

Wellness programs

Mentorship and internal mobility

Job summary

St. Elizabeth HealthCare is seeking a Clinical Research Coordinator to manage and promote clinical studies within the organization and the community. You will screen and enroll participants, coordinate study visits, and ensure regulatory compliance.

Responsibilities include data collection, IRB submissions, informed consent, and collaboration with physicians to open new studies, while maintaining patient privacy and study timelines.

Qualifications

• Understanding of clinical research processes and regulatory requirements.
• Experience coordinating multiple studies and interacting with physicians.
• Ability to adhere to protocol timelines and data integrity standards.

Responsibilities

• Coordinate clinical research studies conducted by the principal investigator.
• Screen and enroll eligible participants and obtain informed consent.
• Coordinate study visits, data collection, and documentation for IRB/ sponsors.
• Ensure compliance with FDA, OHRP, and IRB requirements and maintain study records.

Skills

Coordination

Regulatory knowledge

Data management

Communication skills

Education

Associate degree in related field

Bachelor's degree in related field

Tools

EDC systems

Job description

St. Elizabeth HealthCare is seeking a Clinical Research Coordinator to manage and promote clinical studies within the organization and the community. You will screen and enroll participants, coordinate study visits, and ensure regulatory compliance.

Responsibilities include data collection, IRB submissions, informed consent, and collaboration with physicians to open new studies, while maintaining patient privacy and study timelines.