Senior Clinical Research Coordinator - Grants & Compliance

University of Florida; Gainesville (FL); On-site; USD 65,000 - 90,000; Full time

Benefits offered by this job

Health insurance

Job summary

University of Florida on Main Campus in Gainesville seeks a Clinical Research Coordinator III to oversee the Brooks/PHHP Research Collaboration, coordinating multi-site studies and large grants. You will manage study contracts, budgets, and regulatory submissions with UF contracts & grants, and mentor junior coordinators.

Responsibilities include developing protocols, assessing feasibility, supporting investigators, and ensuring IRB compliance, reporting, and study quality across sites.

Qualifications

• Bachelor's degree in an appropriate area and three years of relevant experience; or an equivalent combination of education and experience.

Responsibilities

• Oversee the budget creation and allocation of multi-million-dollar grants.
• Facilitate negotiation and management of study contracts with UF teams and contracts & grants, PHHP's research administration core, and PT leadership.
• Coordinate record keeping for Brooks/PHHP Research Collaboration studies, including multi-center trials.
• Contribute to development of research funding proposals including protocol development and feasibility assessment.
• Work with Principal Investigators to develop and analyze clinical research activities for participants.
• Educate and mentor research team members and other coordinators.
• Provide regulatory support for approvals (IRB) and ensure compliance across projects.
• Monitor and/or audit studies within the Brooks/PHHP Collaboration.
• Assist in planning and implementing Brooks/PHHP events and coordinating speakers.

Education

Bachelor's degree in an appropriate area

Job description

University of Florida on Main Campus in Gainesville seeks a Clinical Research Coordinator III to oversee the Brooks/PHHP Research Collaboration, coordinating multi-site studies and large grants. You will manage study contracts, budgets, and regulatory submissions with UF contracts & grants, and mentor junior coordinators.

Responsibilities include developing protocols, assessing feasibility, supporting investigators, and ensuring IRB compliance, reporting, and study quality across sites.