Skip to main content
Tallo logoTallo logo
Apply for this opportunity

This job application is on an outside website. Be sure to review the job posting there to verify it's the same.

CLINICAL RESEARCH SITE LIAISON II

Job

Moffitt Cancer Center

Tampa, FL (In Person)

Full-Time

Posted 2 weeks ago (Updated 1 day ago) • Actively hiring

Expires 7/12/2026

Review key factors to help you decide if the role fits your goals.
Pay Growth
?
out of 5
Not enough data
Not enough info to score pay or growth
Job Security
?
out of 5
Not enough data
Calculating job security score...
Total Score
100
out of 100
Average of individual scores

Were these scores useful?

Skill Insights

Compare your current skills to what this opportunity needs—we'll show you what you already have and what could strengthen your application.

Job Description

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.