NTRO RESEARCH COORDINATOR II

H. Lee Moffitt Cancer Center & Research Institute•Tampa, FL

About The Position

Are you looking for an opportunity to be part of an innovative team and make an impact on the lives of those affected by cancer? As a member of the Moffitt Non-Therapeutic Research Office (NTRO) you may interact directly with community members and patients to enroll, educate, and guide participants through the experience of taking part in research. You may support non-therapeutic research in other ways including data entry, project and protocol management and quality assurance. Regardless, you will be a member of a collaborative team that ensures non-therapeutic research activities are moving forward safely, smoothly, and according to plan. Our NTRO Research team comes from a variety of backgrounds and experiences, including public health, psychology, biological sciences and more. There are opportunities for those who have worked in other areas of public health as well as those who are looking for a new and exciting opportunity. Team members of NTRO work closely with community members, patients, patient families, study sponsors, and clinical teams including physicians, pharmacists, nurses, and other health care providers. These positions typically offer a Monday through Friday schedule, though some require occasional weekends. Moffitt offers training and orientation. Position Summary: The primary focus of the NTRO Research Coordinator II is to coordinate one or more non-therapeutic research studies under the GI cancer research portfolio of Drs. Daniel Anaya and Mintallah Haider. Coordination activities include participant recruitment and follow-up, specimen collection, data abstraction and entry. This position is expected to work under general supervision and direction from the Non-Therapeutic Research Office (NTRO) Supervisor to implement and coordinate research, including administrative procedures. This position is part of the NTRO research coordinator (RC) pathway.

Requirements

Associate's degree in Public Health, Psychology, Biological Sciences or relevant field with two (2) years of research experience or relevant experience (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 and one (1) year of research experience or relevant experience (may include time employed in a clinical or laboratory setting including roles such as scribe, clinical scheduling, medical assistant, laboratory or pharmacy technician).
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. https://www.hccfl.edu/academics/subjects/health-and-medical/clinical-research-professional
Master's degree no experience.
Knowledge of research protocols and/or study coordination.
Required general knowledge of medical terminology, general commuter skills (Microsoft Office Suite).
Preferred knowledge of EMR system (PowerChart) and clinical trial management systems (OnCore)
Preferred experience entering data into electronic data capture systems (REDCap or similar)

Nice To Haves

Ability to plan, organize, and coordinate work assignments.
Excellent verbal and written communication skills and the ability to adapt quickly and respond to the study team's needs.
Critical thinking skills and ability to solve issues with minimal guidance.
Continues to build productive internal/external working relationships.
Willingness to pursue phlebotomy certification - Preferred
Preferred knowledge of EMR system (PowerChart) and clinical trial management systems (OnCore)
Preferred experience entering data into electronic data capture systems (REDCap or similar)

Responsibilities

Screen, identify eligibility, and consent participants. This could be any research participant, including community based 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 Electronic Data Capture (EDC) system).
Responsible for quality of the data coming in and ensuring that the protocol is being followed appropriately.
Ensure proper specimen collection at the correct time points, in collaboration with Tissue Core and other stakeholders as appropriate.
Ability to handle a higher volume of moderate complex 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).
Communication involves routinely conveying standardized information to the Regulatory Specialist of study needs; including amendments, new study submissions, and deviations.
Communication involves routinely conveying standardized information with Tissue Core, PRISM, and other shared resources at Moffitt to ensure that the recruitment, data and specimen collection are being coordinated properly.
Research coordinators can contribute to publications and assist with basic publication of results if applicable.