This is a fully remote position, open to applicants in Florida.

📋 Description

• Oversee daily operations for external sites involved in early phase oncology clinical research trials

• Provide support and supervision throughout the entirety of the project life cycle

• Ensure that trial execution adheres to Moffitt standards and aligns with Moffitt processes as well as federal regulations

• Monitor site performance, focusing on enrollment, safety event documentation and reporting, data collection, trend analysis and correction, as well as regulatory tasks

• Manage clinical research initiatives and engage participating stakeholders to facilitate career progression within the career band

⛳️ Requirements

• Associate’s Degree with 5 years of experience in clinical trials involving patient-facing coordination, data management, regulatory, or other research coordination (including 1 year of multi-site experience)

• OR Bachelor’s Degree with 3 years of clinical trials experience in patient-facing coordination, data management, regulatory, or other research coordination (including 1 year of multi-site experience)

• OR Master’s Degree with 1 year of multi-site clinical trials experience in patient-facing coordination, data management, regulatory, or other research coordination

• Oncology experience is preferred

• Familiarity with clinical research regulations and processes