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Summary

The Clinical Research Site Liaison is responsible for the day-to-day management of the activities for external sites participating on early phase oncology clinical research trials. The Clinical Research Site Liaison provides support and oversight for the life cycle of the project, ensuring trial implementation is conducted to Moffitt’s standards and is compliant with Moffitt processes and federal regulations. This position oversees site performance during the execution of the trial including enrollment, safety event recording and reporting, data collection, recognizing and correcting trends, and regulatory activities. The Clinical Research Site Liaison II, is the second level within in career band. Progression to higher levels within the career band reflects increasing depth of professional knowledge, project management, and ability to influence others.

Job Summary: The Clinical Research Site Liaison is responsible for the day-to-day management of the activities for external sites participating on early phase oncology clinical research trials. The Clinical Research Site Liaison provides support and oversight for the life cycle of the project, ensuring trial implementation is conducted to Moffitt’s standards and is compliant with Moffitt processes and federal regulations. This position oversees site performance during the execution of the trial including enrollment, safety event recording and reporting, data collection, recognizing and correcting trends, and regulatory activities. The Clinical Research Site Liaison II, is the second level within in career band. Progression to higher levels within the career band reflects increasing depth of professional knowledge, project management, and ability to influence others. Job Requirements: Requires an Associates Degree plus 5 years clinical trials experience patient facing coordination, data management, regulatory, or other research coordination - preferably in oncology (includes 1 yr multi-site experience) (OR) a Bachelors Degree plus 3 years clinical trials experience patient facing coordination, data management, regulatory, or other research coordination - preferably in oncology (includes 1 yr multi-site experience) (OR) a Master’s Degree plus 1 year multi-site clinical trials experience patient facing coordination, data management, regulatory, or other research coordination - preferably in oncology. Must have knowledge of clinical research regulations and processes.

Salary Range

Salary ranges posted for this position represent the expected base pay range for the role. Actual compensation may vary based on location and a variety of job-related factors, including experience, skills, education, and internal equity among Team Members in similar positions.

We are committed to maintaining fair and equitable pay practices and regularly review compensation to ensure alignment across our workforce.

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