CLINICAL RESEARCH SITE LIAISON II - CTO Partnerships
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.
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.
About the Role
Moffitt has been recognized as a Best and Brightest Company to Work For in the Nation and is continually named one of the Tampa Bay Times’ Top Workplaces. Moffitt has been recognized as a Best and Brightest Company to Work For in the Nation and is continually named one of the Tampa Bay Times’ Top Workplaces.
Qualifications
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.
Skills
Must have knowledge of clinical research regulations and processes.
Benefits
Moffitt has been recognized as a Best and Brightest Company to Work For in the Nation and is continually named one of the Tampa Bay Times’ Top Workplaces.
Pay
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.
Schedule
N/A