Ntro Research Coordinator Ii

## NTRO RESEARCH COORDINATOR IIApply:
Hybrid (Part
-time in Office):
Moffitt Research Center:
Full time:
Posted Today:
R-4406### Working at Moffitt is both a career and a mission: to contribute to the prevention and cure of cancer.### As the only National Cancer Institute-designated Comprehensive Cancer Center based in Florida, Moffitt employs some of the best and brightest minds from around the world. Join a dedicated team of nearly 11,000 who are shaping the future we envision. 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.
** Summary
* * 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:

** This position coordinates research studies within the Hematology Clinic, supporting the majority of Dr. Sallman’s research portfolio. Responsibilities include participant recruitment and follow-up, specimen collection, data abstraction, and data entry. Under the general supervision of the Non-Therapeutic Research Office (NTRO) supervisor, the role supports study implementation, coordination, and administrative activities. This position is part of the NTRO Research Coordinator pathway.
** Ideal Candidate:
*** 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.
** 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 communicate with the proper stakeholders (PI, Regulatory, Management).
* Communication involves routinely conveying standardized information…