Clinical Research Coordinator - Ethical, Patient-Focused Studies

St. Elizabeth Healthcare; Edgewood (KY); On-site; USD 55,000 - 70,000; Full time

Benefits offered by this job

Competitive pay

Health coverage within 30 days

Generous PTO and flexible schedules

Retirement with employer match

Tuition reimbursement

Professional development opportunities

Wellness programs

Internal mobility and mentorship

Job summary

St. Elizabeth Healthcare in Kentucky coordinates clinical research studies for principal investigators and promotes the research program within the community. Responsibilities include screening and enrolling subjects, obtaining informed consents, and ensuring protocol compliance.

Coordinate data collection, regulatory documentation, and IRB submissions while maintaining participant privacy and professional communication with study teams and clinical groups.

Qualifications

• Associate degree in related field with 2 years related experience.
• Bachelor degree in related field.

Responsibilities

• Coordinate clinical research studies for the principal investigators.
• Perform study conduct in accordance with the protocol, SOPs, and operations.
• Collaborate with physicians to open new studies and promote the program within the community.
• Assist in designing recruitment strategies and informed consent processes.
• Provide data collection and submission for sponsors; ensure regulatory compliance.
• Assist with IRB submissions and study document maintenance.
• Screen and enroll potentially eligible participants and manage visits.
• Maintain participant privacy and study chart integrity.

Skills

Clinical research

Participant enrollment

IRB coordination

Data management

Education

Associate degree in related field

Bachelor's degree in related field

Job description

St. Elizabeth Healthcare in Kentucky coordinates clinical research studies for principal investigators and promotes the research program within the community. Responsibilities include screening and enrolling subjects, obtaining informed consents, and ensuring protocol compliance.

Coordinate data collection, regulatory documentation, and IRB submissions while maintaining participant privacy and professional communication with study teams and clinical groups.