NTRO Research Coordinator II

Position Summary

The primary focus of the position is to participate in recruitment, inclusive of specimen and data collecting. Additional duties include coordinating studies of moderate complexity for assigned protocol(s).

Responsibilities

• Screen, identify eligibility, and consent participants.
• Enters data and other pertinent information into the appropriate databases (i.e., Redcap, Power chart, Oncore, sponsor specific EDC system).
• Ensures the protocol is being followed appropriately and the quality of the data coming in is maintained.
• Ensures proper specimen collection at the correct time points, in collaboration with Tissue Core and other stakeholders as appropriate.
• 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.
• Communicates with Tissue Core, PRISM, and other shared resources at Moffitt to ensure that the recruitment, data and specimen collection are being coordinated properly.

Qualifications

• Associate’s degree in Public Health, Psychology, Biological Sciences or relevant field with two (2) years of research or relevant experience required (may include time employed in a clinical or laboratory setting including roles such as scribe, clinical scheduling, medical assistant, laboratory or pharmacy technician); OR Bachelor’s degree requires at least one (1) year of research or relevant experience; OR Master’s degree no experience.
• A Hillsborough Community College (HCC) Associate Degree in Clinical Research can apply towards one (1) year of required research experience. This degree is 60 credit hours.
• Required knowledge of research protocols and/or study coordination.
• Required general knowledge of medical terminology, general commuter skills (Microsoft Office Suite).

Preferred Knowledge and 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).

Benefits

• Moffitt Team Members are eligible for Medical, Dental, Vision, Paid Time Off, Retirement, Parental Leave and more.