NTRO RESEARCH COORDINATOR I

Summary

The primary focus of the position is participant recruitment, inclusive of specimen and data collecting. Additional duties include coordinating studies of lower complexity and other study duties pertaining to assigned protocol(s).

Responsibilities

• Screen, identify eligibility, and consent any research participants including community based and/or clinically based participants depending on the study needs.
• Enters data and other pertinent information into the appropriate databases (i.e., Redcap, Power chart, Oncore, sponsor specific EDC system); Responsible for quality of the data coming in and ensuring that the protocol is being followed appropriately.
• Documents the consent process accurately pursuant to regulatory and Moffitt guidelines.
• Ensure proper specimen collection at the correct time points, in collaboration with Tissue Core and other stakeholders as appropriate.
• Responsible for surveys and/or interviews for some studies.
• Updates protocols with PI’s guidance for submission to the Regulatory Specialist.
• Documents deviations timely and communicates with the proper stakeholders (PI, Regulatory, Management).
• Communicates with the Regulatory Specialist on needs for the study; includes but is not limited to amendments, new study submissions, and deviations.

Qualifications

• Associate’s degree in Public Health, Psychology, Biological Sciences, or relevant field required, Bachelor’s degree preferred.
• Required general knowledge of medical terminology, general computer skills (Microsoft Office Suite).
• Preferred direct research experience.
• Preferred knowledge of EMR system (Powerchart) and clinical trial management systems (OnCore).
• Preferred experience entering data into electronic data capture systems (RedCAP or similar).