Clinical Research Coordinator II — OB/GYN Trials & Compliance

University of Florida; Jacksonville (FL); On-site; USD 65,000 - 80,000; Full time

Job summary

University of Florida in Jacksonville seeks a Clinical Research Coordinator II to oversee coordination of OB/GYN clinical studies. The role serves as the primary contact for research activities, ensuring compliant, timely progresses with multiple stakeholders.

The CRC II will prepare faculty biosketches, assist residents with IRB processes, manage invoicing and budgeting with study sponsors, and support scholarly activity events while traveling as needed.

Qualifications

• Bachelor's degree in an appropriate area and two years of relevant experience; or an equivalent combination of education and experience.
• Experience coordinating clinical research projects or equivalent responsibilities.
• Familiarity with regulatory requirements and informed consent documents.

Responsibilities

• Coordinate clinical research activities within the OB/GYN department.
• Assist residents with IRB navigation and presentation development for compliance.
• Monitor deadlines and maintain documentation for study projects.
• Prepare biosketches for faculty and identify scholarly activity opportunities.
• Collaborate on budgeting, invoicing, and sponsor communications.

Skills

Coordination

IRB navigation

Biosketch preparation

Stakeholder liaison

Education

Bachelor's degree + 2 years experience

Job description

University of Florida in Jacksonville seeks a Clinical Research Coordinator II to oversee coordination of OB/GYN clinical studies. The role serves as the primary contact for research activities, ensuring compliant, timely progresses with multiple stakeholders.

The CRC II will prepare faculty biosketches, assist residents with IRB processes, manage invoicing and budgeting with study sponsors, and support scholarly activity events while traveling as needed.