Clinical Trials Coordinator – Start-Up & Study Ops

University of Central Florida; Orlando (FL); On-site; USD 56,000 - 69,000; Full time

Benefits offered by this job

Medical, dental, vision, life benefits

Paid time off and holidays

Retirement savings options

Employee discounts

Education assistance

Job summary

The University of Central Florida College of Medicine seeks an experienced clinical research professional to support the Manager-Clinical Trials in business development, start-up, quality assurance, study operations, and study closure for clinical research projects and clinical trials.

Responsibilities include building sponsor relationships, navigating start-up and close-out processes, preparing regulatory submissions, budgeting, and ensuring compliance with GCP and regulatory requirements.

Qualifications

• Bachelor's or Master's degree and 2+ years of relevant experience.
• Experience with IRB/IRB submissions and regulatory reporting.
• Strong communication and project coordination skills.
• Familiarity with Good Clinical Practice guidelines.

Responsibilities

• Assist Manager-Clinical Trials in start-up, QA, and study operations.
• Coordinate with sponsors, monitors, and auditors for site visits.
• Support budgeting, contracts, and regulatory applications.

Skills

Regulatory knowledge

Budgeting experience

Sponsor communications

Study coordination

Education

Bachelor's or Master's degree in a relevant field

Job description

The University of Central Florida College of Medicine seeks an experienced clinical research professional to support the Manager-Clinical Trials in business development, start-up, quality assurance, study operations, and study closure for clinical research projects and clinical trials.

Responsibilities include building sponsor relationships, navigating start-up and close-out processes, preparing regulatory submissions, budgeting, and ensuring compliance with GCP and regulatory requirements.